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131818-17-2

131818-17-2 Structure

131818-17-2 Structure
IdentificationMore
[Name]

TERT-BUTYL N-(4-BROMOPHENYL)-CARBAMATE
[CAS]

131818-17-2
[Synonyms]

N-BOC-4-BROMOANILINE
N-BOC-4-bromoaniline, 95+%
4-Bromoaniline, N-BOC protected
TERT-BUTYL 4-BROMOPHENYLCARBAMATE
TERT-BUTYL N-(4-BROMOPHENYL)-CARBAMATE
N-(TERT-BUTOXYCARBONYL)-4-BROMOANILINE
tert-butyl 5-bromopyrazin-2-ylcarbamate
(4-Bromophenyl)carbamic acid tert-butyl ester
TERT-BUTYL N-(4-BROMOPHENYL)-CARBAMATE USP/EP/BP
Carbamic acid, N-(4-bromophenyl)-, 1,1-dimethylethyl ester
[Molecular Formula]

C11H14BrNO2
[MDL Number]

MFCD01006612
[Molecular Weight]

272.14
[MOL File]

131818-17-2.mol
Chemical PropertiesBack Directory
[Melting point ]

103-106 °C(lit.)
[Boiling point ]

281.1±23.0 °C(Predicted)
[density ]

1.398
[Fp ]

124℃
[storage temp. ]

Sealed in dry,2-8°C
[form ]

Powder
[pka]

12.99±0.70(Predicted)
[color ]

Beige
[InChI]

InChI=1S/C11H14BrNO2/c1-11(2,3)15-10(14)13-9-6-4-8(12)5-7-9/h4-7H,1-3H3,(H,13,14)
[InChIKey]

VLGPDTPSKUUHKR-UHFFFAOYSA-N
[SMILES]

C(OC(C)(C)C)(=O)NC1=CC=C(Br)C=C1
[CAS DataBase Reference]

131818-17-2(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HS Code ]

29242990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

N-(tert-Butoxycarbonyl)-4-bromoaniline is an N-(tert-butyloxycarbonyl) [N-BOC] protected 4-bromo aniline. Due to the presence of BOC protection, it serves as an ideal substrate for Suzuki coupling reactions. It affords biaryls via reaction with pyridine or 3-benzaldehyde boronic acids.
[General Description]

N-(tert-Butoxycarbonyl)-4-bromoaniline is an N-(tert-butyloxycarbonyl) [N-BOC] protected 4-bromo aniline. Due to the presence of BOC protection, it serves as an ideal substrate for Suzuki coupling reactions. It affords biaryls via reaction with pyridine or 3-benzaldehyde boronic acids.
Spectrum DetailBack Directory
[Spectrum Detail]

TERT-BUTYL N-(4-BROMOPHENYL)-CARBAMATE(131818-17-2)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

131818-17-2(sigmaaldrich)
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