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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

b-D-Galactopyranoside, 5-bromo-6-chloro-1H-indol-3-yl

OC[C@H]1O[C@@H](Oc2c[nH]c3c2cc(Br)c(c3)Cl)[C@@H]([C@H]([C@H]1O)O)O Request for Quotation
Chemical Name: b-D-Galactopyranoside, 5-bromo-6-chloro-1H-indol-3-yl
CAS Number: 93863-88-8
Product Number: AG003MJO(AGN-PC-0W3I5X)
Synonyms:
MDL No:
Molecular Formula: C14H15BrClNO6
Molecular Weight: 408.6290

Identification/Properties

Properties
MP:
187-191°C
BP:
673.9 °C at 760 mmHg
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
408.629g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
3
Exact Mass:
406.977g/mol
Monoisotopic Mass:
406.977g/mol
Topological Polar Surface Area:
115A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
421
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
5
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H320-H336-H370
Precautionary Statements:
P260-P264-P270-P271-P304+P340+P312-P305+P351+P338+P337+P313-P307+P311-P403+P233-P405-P501
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-6-chloro-3-indolyl-beta-D-galactoside is a valuable chemical compound widely used in chemical synthesis as a chromogenic substrate for the detection of beta-galactosidase activity. This substrate is particularly useful in molecular biology and biochemistry research for the visualization and quantification of gene expression and enzyme activity. In the presence of beta-galactosidase, 5-Bromo-6-chloro-3-indolyl-beta-D-galactoside is hydrolyzed to yield a blue product, enabling the easy and rapid identification of positive reactions. Its sensitivity, specificity, and stability make it a preferred substrate for various applications, including gene expression analysis, reporter gene assays, and enzyme activity assays.