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CAS

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3312-84-3

Glycine, N-[(diphenylmethoxy)carbonyl]-, also known as Z-Gly-OH or Carbobenzyloxy glycine, is a chemical compound derived from the amino acid glycine. It is a white crystalline solid with the molecular formula C16H15NO3 and a molecular weight of 267.29 g/mol. Glycine, N-[(diphenylmethoxy)carbonyl]- is widely used in peptide synthesis as a protecting group for the amino group of glycine residues, preventing unwanted side reactions and ensuring the correct sequence of amino acids in the final peptide product. The carbobenzyloxy (Cbz) group is a common protecting group that can be easily removed under mild acidic conditions, allowing for the deprotection of the glycine residue and the continuation of peptide synthesis. Z-Gly-OH is an essential component in the field of organic chemistry, particularly in the synthesis of peptides, pharmaceuticals, and other bioactive molecules.

3312-84-3

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3312-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3312-84-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,1 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3312-84:
(6*3)+(5*3)+(4*1)+(3*2)+(2*8)+(1*4)=63
63 % 10 = 3
So 3312-84-3 is a valid CAS Registry Number.

3312-84-3Upstream product

3312-84-3Downstream Products

3312-84-3Relevant articles and documents

Use of 2-pyrimidine thiol carbonates as acylating agents for amino or imino containing compounds

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, (2008/06/13)

Thiolcarbonates represented by the formula, SPC1 Wherein R1 and R2 are individually a hydrogen atom or a methyl group, and R3 is a straight chain or branched chain saturated or unsaturated alkyl group having 1 to 5 carbon atoms or is a benzyl or benzhydryl group which may be nuclear substituted, are quite useful for protecting the amino or imino groups of amines, hydrazines, amino acids and peptides with groups of the formula EQU1 The thiolcarbonates can be easily produced by reacting an alkali metal salt of 2-mercaptopyrimidine with phosgene, and reacting the resulting thiolchloroformate with an alcohol (R3 OH), or by reacting a 2-mercaptopyrimidine with a halocarbonic acid ester.

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