125328-77-0

Basic information

• Product Name: 6-acetamido-3-bromo-2-chloro-benzoic acid
• Synonyms: 6-Acetamido-3-bromo-2-chlorobenzoic acid; benzoic acid, 6-(acetylamino)-3-bromo-2-chloro-
• CAS NO: 125328-77-0
• Molecular Formula: C₉H₇BrClNO₃
• Molecular Weight: 292.51
• Mol File: 125328-77-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 469.8°C at 760 mmHg
• Flash Point: 237.9°C
• Density: 1.792g/cm³
• Vapor Pressure: 1.25E-09mmHg at 25°C
• Refractive Index: 1.657
• CAS DataBase Reference: 6-acetamido-3-bromo-2-chloro-benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 6-acetamido-3-bromo-2-chloro-benzoic acid(125328-77-0)
• EPA Substance Registry System: 6-acetamido-3-bromo-2-chloro-benzoic acid(125328-77-0)

Safety Data

• Hazardous Substances Data: 125328-77-0(Hazardous Substances Data)

Upstream product

• 7463-35-6 N-(3-chloro-2-methylphenyl)acetamide 
• 87-60-5 3-chloro-2-methylbenzenamine 
• 125328-80-5 N-(4-bromo-3-chloro-2-methylphenyl)acetamide 
• 627531-47-9 4-amino-2-chloro-3-methylbromobenzene 

Downstream Products

• 1447125-25-8 C₁₅H₁₅BrClNO₄ 
• 125328-84-9 (5-Bromo-4-chloro-indol-3-yl)-β-L-fucopyranoside 
• 153248-52-3 5-bromo-4-chloro-indol-3-yl-(5-acetamido-3,5-dideoxy-α-D-glycero-D-galacto-2-nonulopyranosylonic acid) 
• 3030-19-1 2-amino-5-bromo-6-chlorobenzoic acid 
• 7240-90-6 5-bromo-4-chloro-3-indolyl β-D-galactopyranoside 
• 1607828-63-6 (5-bromo-4-chloroindol-3-yl) (β-D-galactopyranosyl)-(1→4)-β-D-glucopyranoside 
• 6388-45-0 5-bromo-6-chloro-N-[(methoxycarbonyl)methyl]anthranilic acid methyl ester 

Relevant articles and documents

Synthetic method 5- of -4- (-1- I -3-)-(C)-(C)-ethyl-methyl-indol. (by machine translation)

To the method, the 3 - indole chromogenic 5 - substrate is obtained, by hydrolyzing the indole phenol with acetic. anhydride, under an acidic condition with acetic, anhydride to form an indole, chromogenic substrate by hydrolyzing the, indole phenol, with acetic anhydride under an acidic, condition with acetic anhydride under an acidic condition 5 - 5 . (by machine translation)

Novel efficient routes to indoxyl glycosides for monitoring glycosidase activities

A new efficient synthesis for broad access to indoxyl glycosides was developed. Indoxylic acid allyl ester linked to a sugar structure served as the key intermediate in this route. Selective ester cleavage and mild decarboxylation led to the corresponding indoxyl glycosides in good yields. This synthesis was applied for preparation of indoxyl glycosides of fucose, sialic acid, and 6′-sialyl lactose.