CAS 919295-79-7

1H-Indole-3-acetic acid, 6-bromo-, ethyl ester

Description:

1H-Indole-3-acetic acid, 6-bromo-, ethyl ester, with the CAS number 919295-79-7, is a synthetic compound that belongs to the class of indole derivatives. This substance is characterized by its indole core structure, which is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. The presence of a bromo substituent at the 6-position of the indole ring introduces halogen characteristics, which can influence the compound's reactivity and biological activity. The ethyl ester functional group enhances its solubility and may affect its permeability in biological systems. This compound is of interest in various fields, including plant biology, where it may function as a plant growth regulator, mimicking the action of natural auxins. Its potential applications in agricultural science and biochemistry make it a subject of research for understanding plant growth and development mechanisms. As with many chemical substances, safety and handling precautions should be observed due to potential biological activity and toxicity.

Formula: C₁₂H₁₂BrNO₂

InChI: InChI=1S/C12H12BrNO2/c1-2-16-12(15)5-8-7-14-11-6-9(13)3-4-10(8)11/h3-4,6-7,14H,2,5H2,1H3

InChI key: InChIKey=DBEHTVLBNORKMZ-UHFFFAOYSA-N

SMILES: C(C(OCC)=O)C=1C=2C(NC1)=CC(Br)=CC2

Synonyms:

• Ethyl 6-bromo-1H-indole-3-acetate
• 1H-Indole-3-acetic acid, 6-bromo-, ethyl ester
• Ethyl 2-(6-bromo-1H-indol-3-yl)acetate

Ethyl 2-(6-bromo-1H-indol-3-yl)acetate

CAS: 919295-79-7

Versatile small molecule scaffold

Formula: C₁₂H₁₂BrNO₂

Purity: Min. 95%

Molecular weight: 282.13 g/mol

Ref: 3D-ULB29579