CAS 153248-52-3
:BCIN
Description:
BCIN, or 2-bromo-4'-chloro-5'-nitroacetanilide, is a chemical compound characterized by its specific functional groups and structural features. It typically appears as a solid at room temperature and is known for its applications in various fields, including pharmaceuticals and agrochemicals. The presence of bromine, chlorine, and nitro groups in its structure contributes to its reactivity and potential biological activity. BCIN may exhibit properties such as moderate solubility in organic solvents and limited solubility in water, which is common for halogenated compounds. Its molecular structure suggests potential uses in synthesis and as an intermediate in chemical reactions. Safety data sheets would indicate necessary precautions for handling, as compounds with halogenated groups can pose environmental and health risks. Overall, BCIN is a compound of interest in chemical research, particularly for its synthetic utility and potential applications in medicinal chemistry.
Formula:C19H22BrClN2O9
InChI:InChI=1S/C19H22BrClN2O9/c1-7(25)23-15-10(26)4-19(18(29)30,32-17(15)16(28)11(27)6-24)31-12-5-22-9-3-2-8(20)14(21)13(9)12/h2-3,5,10-11,15-17,22,24,26-28H,4,6H2,1H3,(H,23,25)(H,29,30)/t10-,11+,15+,16+,17+,19+/m0/s1
InChI key:InChIKey=YYWCAOZKVRMNIQ-QZUCQFSHSA-N
SMILES:O([C@@]1(C(O)=O)O[C@@]([C@@H]([C@@H](CO)O)O)([C@H](NC(C)=O)[C@@H](O)C1)[H])C=2C=3C(NC2)=CC=C(Br)C3Cl
Synonyms:- D-glycero-α-D-galacto-2-Nonulopyranosidonic acid, 5-bromo-4-chloro-1H-indol-3-yl 5-(acetylamino)-3,5-dideoxy-
- α-Neuraminic acid, N-acetyl-2-O-(5-bromo-4-chloro-1H-indol-3-yl)-
- BCIN
- N-Acetyl-2-O-(5-bromo-4-chloro-1H-indol-3-yl)-α-neuraminic acid
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Found 2 products.
(2S,4S,5R,6R)-5-Acetamido-2-((5-bromo-4-chloro-1H-indol-3-yl)oxy)-4-hydroxy-6-((1R,2R)-1,2,3-trihydroxypropyl)tetrahydro-2H-pyran-2-carboxylic acid
CAS:Formula:C19H22BrClN2O9Molecular weight:537.74305-Bromo-4-chloro-3-indolyl N-acetyl-a-D-neuraminic acid ammonium salt
CAS:<p>5-Bromo-4-chloro-3-indolyl N-acetyl-a-D-neuraminic acid ammonium salt is a substrate used to detect and quantify sialidase activity. Sialidases are enzymes that cleave sialic acid residues from glycoconjugates, and their activity is important in various cellular processes. The substrate is commonly used in research aimed at understanding the role of sialidases in diseases such as influenza and cancer.</p>Formula:C19H22BrClN2O9·NH3·2H2OPurity:Min. 95%Color and Shape:PowderMolecular weight:590.8 g/mol

