59283-35-1

Basic information

• Product Name: (1-benzyl-5-methoxy-2-methyl-1H-indol-3-yl)acetic acid
• CAS NO: 59283-35-1
• Molecular Formula: C₁₉H₁₉NO₃
• Molecular Weight: 309.3591
• Mol File: 59283-35-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 540.9°C at 760 mmHg
• Flash Point: 280.9°C
• Density: 1.17g/cm³
• Vapor Pressure: 1.57E-12mmHg at 25°C
• Refractive Index: 1.593
• CAS DataBase Reference: (1-benzyl-5-methoxy-2-methyl-1H-indol-3-yl)acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (1-benzyl-5-methoxy-2-methyl-1H-indol-3-yl)acetic acid(59283-35-1)
• EPA Substance Registry System: (1-benzyl-5-methoxy-2-methyl-1H-indol-3-yl)acetic acid(59283-35-1)

Safety Data

• Hazardous Substances Data: 59283-35-1(Hazardous Substances Data)

Usage

General Description

(1-benzyl-5-methoxy-2-methyl-1H-indol-3-yl)acetic acid is a chemical compound with a complex structure that includes a benzyl group, a methoxy group, a methyl group, and an indol-3-yl group attached to an acetic acid molecule. (1-benzyl-5-methoxy-2-methyl-1H-indol-3-yl)acetic acid is likely to have a variety of biological activities due to its structure, including potentially acting as a ligand for various receptors in the body. The presence of the benzyl and methoxy groups suggests that this compound may have some level of lipophilicity, which could affect its distribution and metabolism in the body. The specific biological effects and potential applications of this compound would need to be studied in further detail.

Upstream product

• 163734-87-0 (1-Benzyl-5-methoxy-2-methyl-1H-indol-3-yl)-acetic acid benzyl ester 
• 2882-15-7 5-Methoxy-2-methylindole-3-acetic acid 
• 3471-32-7 4-Methoxyphenylhydrazine 
• 100-44-7 benzyl chloride 
• 624-45-3 levulinic acid methyl ester 
• 5705-10-2 N-benzyl-N-(4-methoxy-phenyl)-hydrazine; hydrochloride 

Downstream Products

• 172595-31-2 8-[[5-Methoxy-1-benzyl-2-methyl-1H-indol-3-yl]-acetylamino]-octanoic acid methyl-butyl-amide 
• 441-91-8 2-(1-benzyl-5-methoxy-2-methyl-indol-3-yl)-ethylamine 
• 185501-86-4 4-(1-Benzyl-3-methoxycarbonylmethyl-2-methyl-1H-indol-5-yloxy)-butyric acid ethyl ester 
• 164084-38-2 2-[[3-(2-amino-2-oxoethyl)-2-methyl-1-(phenylmethyl)-1H-indol-5-yl]oxy]acetic acid ethyl ester 
• 164083-73-2 5-(carbethoxymethoxy)-2-methyl-1-(phenylmethyl)-1H-indole-3-acetic acid 
• 163735-05-5 5-hydroxy-2-methyl-1-(phenylmethyl)-1H-indole-3-acetic acid methyl ester 
• 163735-06-6 2-(1-benzyl-5-hydroxy-2-methyl-1H-indol-3-yl)acetic acid 
• 57846-28-3 (1-benzyl-5-methoxy-2-methyl-indol-3-yl)-acetic acid methyl ester 
• 110147-46-1 (1-benzyl-5-methoxy-2-methyl-indol-3-yl)-acetic acid dimethylamide 
• 14075-46-8 [2-(1-benzyl-5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine 
• 97077-43-5 3-(amidomethyl)-2-methyl-1-(phenylmethyl)-5-methoxyindole 
• 909390-30-3 ethyl 2-(2-(1-benzyl-5-methoxy-2-methyl-1H-indol-3-yl)acetamido)acetate 

Relevant articles and documents

Synthesis of amino acid derivatives of indole-3-acetic acid

Amino acid derivatives of a modified indole-3-acetic acid have been synthesised. Fourteen new dipeptide-like compounds 3-4 were obtained and their structures were elucidated based on the IR, 1H NMR, MS spectra.

1H-INDOLE-3-ACETAMIDE SPLA2 INHIBITORS

A class of novel 1-indole-3-acetamides represented by the formula; is disclosed together with the use of such indole compounds for inhibiting sPLA2 mediated release of fatty acids.

1H-INDOLE-3-ACETIC ACID HYDRAZIDE SPLA2 INHIBITORS

A class of novel 1H-indole-3-acetic acid hydrazides is disclosed together with the use of such indole compounds for inhibiting sPLA2 mediated release of fatty acids (e.g., arachidonic acid) for treatment of conditions such as septic shock