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96551-21-2

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96551-21-2 Structure

96551-21-2 Structure
IdentificationBack Directory
[Name]

TERT-BUTYL 3-BROMOMETHYL-INDOLE-1-CARBOXYLATE
[CAS]

96551-21-2
[Synonyms]

3-(Bromomethyl)-1H
3-BROMOMETHYL-1-TERT-BUTOXYCARBONYLINDOLE
t-Butyl-3-bromomethylindole-1-carboxylate
3-(Bromomethyl)-1H-indole, N-BOC protected
1-(t-butyloxycarbonyl)-3-(bromomethyl)indole
TERT-BUTYL 3-BROMOMETHYL-INDOLE-1-CARBOXYLATE
TERT-BUTYL 3-(BROMOMETHYL)-1H-INDOLE-1-CARBOXYLATE
3-BROMOMETHYL-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
1H-Indole-1-carboxylic acid, 3-(bromomethyl)-, 1,1-dimethylethyl ester
tert-Butyl 3-(bromomethyl)-1H-indole-1-carboxylate, 3-(Bromomethyl)-1-(tert-butoxycarbonyl)-1H-indole
[Molecular Formula]

C14H16BrNO2
[MDL Number]

MFCD05864361
[MOL File]

96551-21-2.mol
[Molecular Weight]

310.19
Chemical PropertiesBack Directory
[Melting point ]

106 °C
[Boiling point ]

391.1±34.0 °C(Predicted)
[density ]

1.34±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P280-P305+P351+P338-P310
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

tert-Butyl 3-(bromomethyl)-1H-indole-1-carboxylate is used as a reactant in the preparation of α,α-dialkyl-α-amino acids via enantioselective alkylation of amino acid Schiff bases.
Spectrum DetailBack Directory
[Spectrum Detail]

TERT-BUTYL 3-BROMOMETHYL-INDOLE-1-CARBOXYLATE(96551-21-2)1HNMR
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