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23446-03-9

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23446-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23446-03-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,4,4 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23446-03:
(7*2)+(6*3)+(5*4)+(4*4)+(3*6)+(2*0)+(1*3)=89
89 % 10 = 9
So 23446-03-9 is a valid CAS Registry Number.

23446-03-9SDS

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 BOC-MET-GLY-OH

1.2 Other means of identification

Product number -
Other names N-t-butoxycarbonyl-L-methionylglycine

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:23446-03-9 SDS

23446-03-9Relevant academic research and scientific papers

Conjugate addition of thiols and malonates to thiocinnamates under PTC conditions

Marzorati, Liliana,De Mattos, Marcos Carlos,Wladislaw, Blanka,Di Vitta, Claudio

, p. 1427 - 1435 (2002)

Addition of thiols or diethylmalonate to thiocinnamate, under solid-liquid PTC conditions, afforded the corresponding 1,4-adducts in moderate to good yields. A 2-pyrrolidinone was obtained using diethyl N-acetamidomalonate as Michael donor, via intramolecular cyclization of the parent adduct.

Phenylhydrazide as an enzyme-labile protecting group in peptide synthesis

Voelkert, Martin,Koul, Surrinder,Mueller, Gernot H.,Lehnig, Manfred,Waldmann, Herbert

, p. 6902 - 6910 (2007/10/03)

The enzymatic cleavage of amino acid phenylhydrazides with the enzyme tyrosinase (EC 1.14.18.1) offers a new, mild, and selective method for C-terminal deprotection of peptides. The advantages of the described methodology are the very mild oxidative removal of the protecting group at room temperature and pH 7, a high chemo- and regioselectivity, and the availability of the biocatalyst. Even in oxygen-saturated solution, the oxidation of sensitive methionine residues was not observed. These features make the methodology suitable for the synthesis of sensitive peptide conjugates. Mechanistic data suggest that the hydrolysis of the oxidized adducts proceeds by a free-radical mechanism.

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