ChemicalBook--->CAS DataBase List--->27933-36-4

27933-36-4

27933-36-4 Structure

27933-36-4 Structure
IdentificationBack Directory
[Name]

BNPS-SKATOLE
[CAS]

27933-36-4
[Synonyms]

Nsc 240875
BNPS-SKATOL
BNPS-SKATOLE
Einecs 248-737-9
3-bromo-3-methyl-2-(2-nitrophenyl)sulfanylindole
3-Bromo-3-methyl-2-(2-nitrophenylthio)-3H-indole
2-[2'-NITROPHENYLSULFENYL]-3-METHYL-3-BROMOINDOLE
BROMO-3-METHYL-2-(2-NITROPHENYLMERCAPTO)-3H-INDOLE
3-BROMO-3-METHYL-2-(2-NITROPHENYL-MERCAP TO)-3H-IND
2-(2-NITROPHENYLSULFENYL)-3-METHYL-3-BROMOINDOLENINE
2(2-NITROPHENYLSULFENYL)-3-METHYL-3'-BROMOINDOLENINE
2-(2-Nitrophenylsulfenyl)-3-methyl-3-bromo-3H-indole
3H-Indole, 3-bromo-3-methyl-2-((2-nitrophenyl)thio)-
3-BROMO-3-METHYL-2-(2-NITROPHENYLMERCAPTO)-3H-INDOLE
2-(2'-NITROPHENYLSULFENYL)-3-METHYL-3-BROMOINDOENINE
2-[2'-NITROPHENYLSULFENYL]-3-METHYL-3'-BROMOINDOLENINE
2-(2'-NITROPHENYLSULPHENYL)-3-METHYL-3-BROMOINDOLENINE
2-(2-Nitrophenylsulfenyl)-3-methyl-3-bromoindolenine, 3-Bromo-3-methyl-2-(2-nitrophenylmercapto)-3H-indole, BNPS-skatol
[EINECS(EC#)]

248-737-9
[Molecular Formula]

C15H11BrN2O2S
[MDL Number]

MFCD00037978
[MOL File]

27933-36-4.mol
[Molecular Weight]

363.23
Chemical PropertiesBack Directory
[Boiling point ]

448.8±45.0 °C(Predicted)
[density ]

1.57±0.1 g/cm3(Predicted)
[storage temp. ]

−20°C
[pka]

2.45±0.40(Predicted)
[InChI]

InChI=1S/C15H11BrN2O2S/c1-15(16)10-6-2-3-7-11(10)17-14(15)21-13-9-5-4-8-12(13)18(19)20/h2-9H,1H3
[InChIKey]

BXTVQNYQYUTQAZ-UHFFFAOYSA-N
[SMILES]

N1C2=C(C=CC=C2)C(Br)(C)C=1SC1=CC=CC=C1[N+]([O-])=O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P271-P280
[Safety Statements ]

24/25
[WGK Germany ]

3
[F ]

10
[HS Code ]

2933998090
Hazard InformationBack Directory
[Definition]

ChEBI: A bromoindole that is 3H-indole in which the hydrogen at position 2 has been replaced by an (o-nitrophenyl)sulfanyl group and in which the hydrogens at position 3 have been replaced by a bromine and a methyl group. It is use particularly for the selective cleavage of tryptophanyl peptide bonds (cleavage occurs at peptide bonds after amino acids with available Cgamma2Cdelta double bonds su h as tryptophan, tyrosine, and histidine).
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