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Carbamic acid, [(1R)-2-oxo-1-phenylpropyl]-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

833487-57-3

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833487-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 833487-57-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,3,4,8 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 833487-57:
(8*8)+(7*3)+(6*3)+(5*4)+(4*8)+(3*7)+(2*5)+(1*7)=193
193 % 10 = 3
So 833487-57-3 is a valid CAS Registry Number.

833487-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl N-[(1R)-2-oxo-1-phenylpropyl]carbamate

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:833487-57-3 SDS

833487-57-3Downstream Products

833487-57-3Relevant academic research and scientific papers

Convergent approach to (E)-alkene and cyclopropane peptide isosteres

Wipf, Peter,Xiao, Jingbo

, p. 103 - 106 (2007/10/03)

(Chemical Equation Presented) Trisubstituted (E)-alkene isosteres (TEADIs) and novel cyclopropane amide bond isosteres (CPDIs) were synthesized by aldimine addition and three-component aldimine addition-cyclopropanation methodologies, respectively. These

An efficient and enantioselective synthesis of a chiral primary amine

Son, Youngchan,Park, Chihyo,Koh, Jong Sung,Choy, Nakyen,Lee, Chang S.,Choi, Ho-Il,Kim, Sung Chun,Yoon, Heungsik

, p. 3745 - 3746 (2007/10/02)

An efficient and enantioselective method for the preparation of a chiral primary amine has been developed. Starting from N-protected L or D-amino acid the sequence involves coupling with N-methoxy-N-methylamine, acylation, olefination with potassium bis(trimethylsilyl)amide, and hydrogenation.

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