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Z-GLY-DL-ALA-OH, also known as Z-Gly-DL-Alaninol, is a peptide compound consisting of a protected glycine (Z-protected) and a racemic mixture of alanine. The "Z" group is a benzyloxycarbonyl (Cbz) protecting group, which is commonly used in peptide synthesis to prevent unwanted side reactions. The compound is a valuable intermediate in the synthesis of various peptides and pharmaceuticals, as it allows for the controlled formation of peptide bonds. Its racemic nature means that it contains equal amounts of the L- and D-isomers of alanine, which can be important depending on the specific application. Z-GLY-DL-ALA-OH is used in research and development for creating new drugs, vaccines, and other bioactive molecules.

23446-00-6

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23446-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23446-00-6 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 23446-00:
(7*2)+(6*3)+(5*4)+(4*4)+(3*6)+(2*0)+(1*0)=86
86 % 10 = 6
So 23446-00-6 is a valid CAS Registry Number.

23446-00-6SDS

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 N-(N-benzyloxycarbonyl-glycyl)-DL-alanine

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

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More Details:23446-00-6 SDS

23446-00-6Relevant academic research and scientific papers

PEPTIDE BOND FORMATION UNDER PHASE-TRANSFER CONDITIONS. EFFECT OF AMINO ACID STRUCTURE

Kosmynin, V. V.,Kaida, L. N.,Savelova, V. A.,Taran, N. A.

, p. 2306 - 2311 (2007/10/02)

The extraction of amino acids NH2CH(R)COOH in the two-phase system consisting of 1-butanol and an amino acid buffer solution in the presence of cetyltrimethylammonium bromide and also the kinetics of the aminolysis of N-benzyloxycarbonylglycine p-nitrophe

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