Category: 63352-97-6

COA of Formula: C10H8BrNO2. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: 2-(7-Bromo-1H-indol-3-yl)acetic acid, is researched, Molecular C10H8BrNO2, CAS is 63352-97-6, about Growth of Avena coleoptiles and pH drop of protoplast suspensions induced by chlorinated indoleacetic acids.

Several indoleacetic acids, substituted in the benzene ring, were compared in the Avena straight growth bioassay. 4-Chloroindoleacetic acid (I) [2519-61-1], a naturally occurring plant hormone, was one of the strongest hormones in this bioassay. With an optimum at 10-6 mol/L, it was more active than indoleacetic acid [87-51-4], 2,4-dichlorophenoxyacetic acid [94-75-7], and naphthaleneacetic acid [86-87-3]. 5-Chloro- [1912-45-4] and 6-chloroindoleacetic acid [1912-44-3] are very strong auxins as well. Other derivatives tested have a lower activity. 5,7-Dichloro- [1912-40-9] and 5-hydroxyindoleacetic acid [54-16-0] have very low auxin activity at 10-4 mol/L and may be antiauxins. Some of the derivatives were compared for their effect on pH decline in stem protoplast suspensions of Helianthus annuus and Pisum sativum. The change of pH occurs without a lag period or with only a very short one. Derivatives which are very active in the Avena straight growth assay cause a larger pH decline than indoleacetic acid, while inactive derivatives cause effectively no pH decline.

After consulting a lot of data, we found that this compound(63352-97-6)COA of Formula: C10H8BrNO2 can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Thiazolidine – Wikipedia,
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Recommanded Product: 63352-97-6. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: 2-(7-Bromo-1H-indol-3-yl)acetic acid, is researched, Molecular C10H8BrNO2, CAS is 63352-97-6, about Substituted indoleacetic acids tested in tissue cultures. Author is Engvild, Kjeld C..

Monochloro substituted indole-3-acetic acids inhibited shoot induction in tobacco tissue cultures about as much as IAA. Dichloro substituted indole-3-acetic acids inhibited shoot formation less. Other substituted indoleacetic acids except 5-fluoro- and 5-bromoindole-3-acetic acid were less active than IAA. Callus growth was quite variable and not correlated with auxin strength measured in the Avena coleoptile test.

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Product Details of 63352-97-6. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: 2-(7-Bromo-1H-indol-3-yl)acetic acid, is researched, Molecular C10H8BrNO2, CAS is 63352-97-6, about Molecular recognition of indole derivatives by polymers imprinted with indole-3-acetic acid: A QSPR study. Author is Porobic, Ivana; Kontrec, Darko; Soskic, Milan.

Three molecularly imprinted polymers (MIPs) were prepared using the phytohormone indole-3-acetic acid (IAA) as a template mol., 4-vinylpyridine (MIP-1 and MIP-2) or N,N-dimethylaminoethyl methacrylate (MIP-3) as functional monomers, ethylenglycol dimethacrylate as a cross linker and acetonitrile (MIP-1), a methanol-water mixture (MIP-2) or chloroform (MIP-3) as porogens. Retention factors for IAA and 29 indole derivatives were determined by high-performance liquid chromatog., using the molecularly imprinted polymers as stationary phases and acetonitrile as an eluent. High correlations between selectivity factors of above mentioned polymers indicate that their retention mechanisms are basically the same. A quant. structure-property relationships anal. revealed that the presence of the terminal carboxyl group on the 3-side chain plays an essential role in the binding of the indole derivatives to the polymers. The derivatives without the carboxyl group exhibit a drastically lower affinity toward the polymers. Another factor which favors the binding is electronic d. of indole nucleus. Substituents with electro-withdrawing properties enhance the binding, while electro-donating substituents have the opposite effect. The length of the 3-side chain also affects the binding. Indole-3-carboxylic acid having the carboxyl group directly attached to the ring as well as the derivatives whose side chain is longer than that of IAA bind to the polymers with a lower affinity.

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Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com

So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic.Wu, Kui; Du, Yuliu; Wang, Ting researched the compound: 2-(7-Bromo-1H-indol-3-yl)acetic acid( cas:63352-97-6 ).Application of 63352-97-6.They published the article 《Visible-Light-Mediated Construction of Pyrroloindolines via an Amidyl Radical Cyclization/Carbon Radical Addition Cascade: Rapid Synthesis of (±)-Flustramide B》 about this compound( cas:63352-97-6 ) in Organic Letters. Keywords: pyrroloindoline preparation amidyl radical cyclization carbon radical addition cascade; flustramide B synthesis. We’ll tell you more about this compound (cas:63352-97-6).

The development of visible-light-mediated synthesis of pyrrolo[2,3-b]indolines via an amidyl radical cyclization-carbon radical functionalization cascade is reported. The transformation shows a broad substrate scope, tolerating a variety of substitutions on indole aromatic rings and N-centers. Different functionalized alkene systems could be used as radical acceptors. Relying on this strategy, a rapid synthesis of flustramide B was achieved.

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Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com

Katekar, GerardF.; Geissler, Art E. published an article about the compound: 2-(7-Bromo-1H-indol-3-yl)acetic acid( cas:63352-97-6,SMILESS:O=C(O)CC1=CNC2=C1C=CC=C2Br ).HPLC of Formula: 63352-97-6. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:63352-97-6) through the article.

A series of halogenated indoleacetic acids were assessed for auxin activity on pea stem and wheat coleoptile sections. Activity differences between the 2 species were found. These are discussed in terms of differences in receptor models for pea and wheat, with the models differing in the areas covered by the 6- and 7-substituted compounds

Although many compounds look similar to this compound(63352-97-6)HPLC of Formula: 63352-97-6, numerous studies have shown that this compound(SMILES:O=C(O)CC1=CNC2=C1C=CC=C2Br), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com

Category: thiazolidine. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: 2-(7-Bromo-1H-indol-3-yl)acetic acid, is researched, Molecular C10H8BrNO2, CAS is 63352-97-6, about Auxin activity of brominated indoles from the marine sponge Pseudosuberites hyalinus.

A series of brominated indoles from the marine sponge Pseudosuberites hyalinus and 6-bromoindole-3-acetic acid (6-Br-IAA) were assessed for auxin activity in Avena and Triticum straight growth assay. 6-Br-IAA showed low activity compared to 6-chloroindole-3-acetic acid, while the corresponding Me esters had comparable activities.

Although many compounds look similar to this compound(63352-97-6)Category: thiazolidine, numerous studies have shown that this compound(SMILES:O=C(O)CC1=CNC2=C1C=CC=C2Br), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: 2-(7-Bromo-1H-indol-3-yl)acetic acid, is researched, Molecular C10H8BrNO2, CAS is 63352-97-6, about Preparation of chlorinated 3-indolylacetic acids.Product Details of 63352-97-6.

Indoleacetic acids I (Rn = 4-Cl, 6-Cl) were prepared in 38-40% yield by reaction of the resp. chloro(diethylaminomethyl)indole with NaCN followed by hydrolysis. I (Rn = 5-Cl, 7-Cl, 4,6-Cl2, 4,7-Cl2, 5,7-Cl2, 6,7-Cl2, 5-Cl-7-Me, 7-Br) were prepared in 7-28% yield by reaction of HCOCH2CH2CO2H with the appropriate phenylhydrazine hydrochlorides.

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Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: 2-(7-Bromo-1H-indol-3-yl)acetic acid, is researched, Molecular C10H8BrNO2, CAS is 63352-97-6, about Growth of Avena coleoptiles and pH drop of protoplast suspensions induced by chlorinated indoleacetic acids.COA of Formula: C10H8BrNO2.

Several indoleacetic acids, substituted in the benzene ring, were compared in the Avena straight growth bioassay. 4-Chloroindoleacetic acid (I) [2519-61-1], a naturally occurring plant hormone, was one of the strongest hormones in this bioassay. With an optimum at 10-6 mol/L, it was more active than indoleacetic acid [87-51-4], 2,4-dichlorophenoxyacetic acid [94-75-7], and naphthaleneacetic acid [86-87-3]. 5-Chloro- [1912-45-4] and 6-chloroindoleacetic acid [1912-44-3] are very strong auxins as well. Other derivatives tested have a lower activity. 5,7-Dichloro- [1912-40-9] and 5-hydroxyindoleacetic acid [54-16-0] have very low auxin activity at 10-4 mol/L and may be antiauxins. Some of the derivatives were compared for their effect on pH decline in stem protoplast suspensions of Helianthus annuus and Pisum sativum. The change of pH occurs without a lag period or with only a very short one. Derivatives which are very active in the Avena straight growth assay cause a larger pH decline than indoleacetic acid, while inactive derivatives cause effectively no pH decline.

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Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com

Luebbe, Claus; Van Pee, Karl Heinz; Salcher, Olga; Lingens, Franz published an article about the compound: 2-(7-Bromo-1H-indol-3-yl)acetic acid( cas:63352-97-6,SMILESS:O=C(O)CC1=CNC2=C1C=CC=C2Br ).Recommanded Product: 2-(7-Bromo-1H-indol-3-yl)acetic acid. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:63352-97-6) through the article.

P. pyrrocinia ATCC 15958 and a mutant strain (ACN) of P. aureofaciens ATCC 15926 possess a mechanism for the degradation of the tryptophan side chain. Indole, indole-3-carboxylic acid, indole-3-acetic acid, the corresponding compounds chlorinated or brominated at position 7, indole-3-pyruvate, and 7-chloroindole-3-pyruvate were isolated from bacterial cultures. The chlorinated indole derivatives were isolated after the addition of 7-chloro-DL-tryptophan to cultures of P. pyrrocinia whereas their bromo analogs were found in the culture medium of the mutant strain ACN of P. aureofaciens, grown in the presence of NaBr. Enzymic studies show that tryptophan is transaminated to indole-3-pyruvate, which is transformed to indole-3-acetaldehyde. Dehydrogenation of indole-3-acetaldehyde leads to indole-3-acetic acid, which is further metabolized to indole-3-carboxaldehyde and converted by dehydrogenation to indole-3-carboxylic acid. Indole is formed by the spontaneous decarboxylation of indole-3-carboxylic acid.

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In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Preparation of chlorinated 3-indolylacetic acids, published in 1977, which mentions a compound: 63352-97-6, mainly applied to indoleacetic acid chloro; phenylhydrazine cyclization formylpropionate; hydrazine phenyl reaction formylpropionate; propionate formyl reaction phenylhydrazine, SDS of cas: 63352-97-6.

Indoleacetic acids I (Rn = 4-Cl, 6-Cl) were prepared in 38-40% yield by reaction of the resp. chloro(diethylaminomethyl)indole with NaCN followed by hydrolysis. I (Rn = 5-Cl, 7-Cl, 4,6-Cl2, 4,7-Cl2, 5,7-Cl2, 6,7-Cl2, 5-Cl-7-Me, 7-Br) were prepared in 7-28% yield by reaction of HCOCH2CH2CO2H with the appropriate phenylhydrazine hydrochlorides.

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Thiazolidine – Wikipedia,
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