17016-46-5

Basic information

• Product Name: 5-BROMO-4-CHLORO-3-INDOXYL-BETA-D-FUCOPYRANOSIDE
• Synonyms: X-BETA-D-FUC;X-BETA-D-FUCOSIDE;X-FUCOSIDE;5-bromo-4-chloro-3-indolyl B-D-*fucopyranoside;X-fucopyranoside;5-Bromo-4-chloroindol-3-yl-b-D-fucopyranoside;5-Bromo-4-chloro-3-indoxyl-beta-D-fucopyranoside,99%;5-Bromo-4-chloro-3-indolyl β-D-fucopyranoside ,98%
• CAS NO: 17016-46-5
• Molecular Formula: C14H15BrClNO5
• Molecular Weight: 392.63
• EINECS: 1533716-785-6
• Product Categories: ChromogenicEnzyme Substrates;Fucoside;Activity;Fluorogenic;Substrates;substrate
• Mol File: 17016-46-5.mol
• Article Data: 1

Chemical Properties

• Melting Point: 213-217 °C
• Boiling Point: 611℃
• Flash Point: 323℃
• Appearance: /
• Density: 1.796
• Vapor Pressure: 8.63E-16mmHg at 25°C
• Refractive Index: 1.709
• Storage Temp.: −20°C
• CAS DataBase Reference: 5-BROMO-4-CHLORO-3-INDOXYL-BETA-D-FUCOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BROMO-4-CHLORO-3-INDOXYL-BETA-D-FUCOPYRANOSIDE(17016-46-5)
• EPA Substance Registry System: 5-BROMO-4-CHLORO-3-INDOXYL-BETA-D-FUCOPYRANOSIDE(17016-46-5)

Safety Data

• Safety Statements: 24/25
• WGK Germany: 3
• Hazardous Substances Data: 17016-46-5(Hazardous Substances Data)

Usage

Chemical Properties

white to slightly off-white powder

InChI:InChI=1/C14H15BrClNO5/c1-5-11(18)12(19)13(20)14(21-5)22-8-4-17-7-3-2-6(15)10(16)9(7)8/h2-5,11-14,17-20H,1H3/t5-,11+,12+,13-,14+/m1/s1

Upstream product

• 943138-45-2 5-bromo-6-chloro-isatoic anhydride 
• 3030-19-1 2-amino-5-bromo-6-chlorobenzoic acid 
• 7463-35-6 N-(3-chloro-2-methylphenyl)acetamide 
• 87-60-5 3-chloro-2-methylbenzenamine 
• 125328-77-0 N-acetyl-5-bromo-6-chloroanthranilic acid 
• 125328-80-5 N-(4-bromo-3-chloro-2-methylphenyl)acetamide 
• 627531-47-9 4-amino-2-chloro-3-methylbromobenzene 
• 1447125-37-2 (N-acetyl-5-bromo-4-chloro-indol-3-yl)-2,3,4-tri-O-acetyl-β-L-fucopyranoside 
• 1447125-31-6 (5-bromo-4-chloro-indox-3-ylic acid allyl ester)-2,3,4-tri-O-acetyl-β-L-fucopyranoside 
• 1447125-28-1 5-bromo-4-chloroindoxylic acid allyl ester 
• 1447125-25-8 C₁₅H₁₅BrClNO₄ 
• 1447125-22-5 C₁₃H₉BrClNO₅ 

Relevant articles and documents

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.