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Carbamic acid, (2-bromo-2-phenylethyl)-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

358365-87-4

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358365-87-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 358365-87-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,8,3,6 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 358365-87:
(8*3)+(7*5)+(6*8)+(5*3)+(4*6)+(3*5)+(2*8)+(1*7)=184
184 % 10 = 4
So 358365-87-4 is a valid CAS Registry Number.

358365-87-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Boc-2-bromo-2-phenylethylamine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:358365-87-4 SDS

358365-87-4Relevant academic research and scientific papers

Regioselective aminobromination of terminal alkenes

?liwińska, Anna,Zwierzak, Andrzej

, p. 5927 - 5934 (2007/10/03)

The addition of t-butyl N,N-dibromocarbamate (BBC) to a variety of terminal alkenes has been studied. The reaction was spontaneously initiated and proceeded smoothly in refluxing dichloromethane. The N-bromo adducts, formed upon addition, could be reduced

t-Butyl N,N-dibromocarbamate (BBC) - New reagent for aminobromination of terminal alkenes

Klepacz, Anna,Zwierzak, Andrzej

, p. 4539 - 4540 (2007/10/03)

t-Butyl N,N-dibromocarbamate, easily obtained by bromination of t-butyl carbamate in aqueous potassium carbonate, reacts smoothly with a variety of terminal alkenes to afford the corresponding β-bromo-N-Boc-amines upon reduction with aqueous sodium sulphi

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