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146953-81-3

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146953-81-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146953-81-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,9,5 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 146953-81:
(8*1)+(7*4)+(6*6)+(5*9)+(4*5)+(3*3)+(2*8)+(1*1)=163
163 % 10 = 3
So 146953-81-3 is a valid CAS Registry Number.

146953-81-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-(tert-butoxycarbonyl)[(15)N]leucine

1.2 Other means of identification

Product number -
Other names BOC-[15N]LEU-OH

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:146953-81-3 SDS

146953-81-3Downstream Products

146953-81-3Relevant articles and documents

Synthesis of (15)N-Labelled Chiral Boc-Amino Acids from Triflates: Enantiomers of Leucine and Phenylalanine

Degerbeck, Fredrik,Fransson, Bengt,Grehn, Leif,Ragnarsson, Ulf

, p. 11 - 14 (2007/10/02)

An efficient synthesis of (15)N-labelled chiral Boc-amino acids by triflate alkylation of di-tert-butyl iminodicarbonate is reported.Both enantiomers of Boc-Leucine and -phenylalanine were synthesized from commercial α-amino acids of opposite configuration via α-hydroxy carboxylic acids provided by diazotization, thus extending the scope of an earlier exploratory study.The high chiral purity of the final products was confirmed by HPLC.These labelled amino acid derivatives are suitable for direct application to the synthesis of labelled peptides.

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