| Identification | More | [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 Properties | Back 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 Data | Back Directory | [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 Information | Back 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. |
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