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L-Leucine, N-(bromophenylacetyl)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

620179-30-8

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620179-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 620179-30-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,0,1,7 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 620179-30:
(8*6)+(7*2)+(6*0)+(5*1)+(4*7)+(3*9)+(2*3)+(1*0)=128
128 % 10 = 8
So 620179-30-8 is a valid CAS Registry Number.

620179-30-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-N-(α-bromo-α-phenylacetyl)leucine methyl ester

1.2 Other means of identification

Product number -
Other names N-(α-bromo-α-phenylacetyl)-L-leucine methyl ester

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:620179-30-8 SDS

620179-30-8Downstream Products

620179-30-8Relevant academic research and scientific papers

Asymmetric nucleophilic substitution of α-bromo amides via dynamic kinetic resolution for the preparation of dipeptide analogues

Nam, Jiyoun,Chang, Ji-Yeon,Shin, Eun-Kyoung,Kim, Hyun Jung,Kim, Yangmee,Jang, Soonmin,Park, Yong Sun

, p. 6311 - 6318 (2004)

Asymmetric nucleophilic substitution reactions of α-bromo α-aryl acetamides derived from L-amino acids are described. The simple and practical syntheses of dipeptide analogues have been developed with dibenzylamine, TBAI and a base to provide 2a-2n and 4

Stereoselective syntheses of tri- and tetrapeptide analogues by dynamic resolution of α-halo amides in nucleophilic substitution

Chang, Ji-Yeon,Shin, Eun-Kyoung,Kim, Hyun Jung,Kim, Yangmee,Park, Yong Sun

, p. 2743 - 2750 (2007/10/03)

Dynamic resolution of α-bromo and α-chloro acetamides in nucleophilic substitution with amine nucleophiles in the presence of TBAI has been investigated for stereoselective syntheses of tri- and tetrapeptide analogues. Mechanistic investigations suggest t

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