5-Bromo-4-chloro-3-indolyl-beta-D-glucoside

Modify Date: 2024-01-06 12:53:32

5-Bromo-4-chloro-3-indolyl-beta-D-glucoside Structure
5-Bromo-4-chloro-3-indolyl-beta-D-glucoside structure
Common Name 5-Bromo-4-chloro-3-indolyl-beta-D-glucoside
CAS Number 15548-60-4 Molecular Weight 407.622
Density 1.882 g/cm3 Boiling Point 698.0±55.0 °C at 760 mmHg
Molecular Formula C14H15BrClNO6 Melting Point 249-251ºC
MSDS USA Flash Point 375.9±31.5 °C

 Use of 5-Bromo-4-chloro-3-indolyl-beta-D-glucoside


5-Bromo-4-chloro-3-indolyl β-D-Glucopyranoside is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name 5-bromo-4-chloro-3-indolyl β-D-glucoside
Synonym More Synonyms

  Biological Activity

Description 5-Bromo-4-chloro-3-indolyl β-D-Glucopyranoside is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog

 Chemical & Physical Properties

Density 1.882 g/cm3
Boiling Point 698.0±55.0 °C at 760 mmHg
Melting Point 249-251ºC
Molecular Formula C14H15BrClNO6
Molecular Weight 407.622
Flash Point 375.9±31.5 °C
Exact Mass 405.969849
PSA 115.17000
LogP 1.50
Vapour Pressure 0.0±2.3 mmHg at 25°C
Index of Refraction 1.731

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 29389090

 Articles5

More Articles
SUBSTRATES FOR CYTOCHEMICAL DEMONSTRATION OF ENZYME ACTIVITY. I. SOME SUBSTITUTED 3-INDOLYL-BETA-D-GLYCOPYRANOSIDES.

J. Med. Chem. 7 , 574, (1964)

Novel compound for identifying Escherichia coli.

Appl. Environ. Microbiol. 54(7) , 1874-5, (1988)

A new chromogenic compound, 5-bromo-4-chloro-3-indoxyl-beta-D-glucuronide, was found to be useful for the rapid, specific, differential identification of Escherichia coli in the sanitary analysis of s...

Chemiluminescent assay of various enzymes using indoxyl derivatives as substrate and its applications to enzyme immunoassay and DNA probe assay.

Anal. Biochem. 199(2) , 238-42, (1991)

Chemiluminescent assays of various enzymes have been developed using indoxyl derivatives as substrates. The principle of the method is as follows: an enzyme causes hydrolysis of an indoxyl derivative ...

 Synonyms

MFCD00063690
5-Bromo-4-chloro-3-indolyl-β-D-glucoside
β-D-Glucopyranose, 2-O-(5-bromo-4-chloro-1H-indol-3-yl)-, ion(1-)
5-bromo-4-chloro-3-indolyl beta-D-glucoside
(2R,3R,4S,5S,6R)-3-[(5-Bromo-4-chloro-1H-indol-3-yl)oxy]-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-olate
X-Glc X-glucoside
EINECS 239-603-0