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H-Gly-Ser-OBzl, also known as Z-Gly-Ser-OH or benzyloxycarbonyl-glycyl-seryl, is a tripeptide consisting of three amino acids: glycine (Gly), serine (Ser), and a terminal hydroxyl group (OH) protected by a benzyl group (OBzl). This chemical structure is commonly used in peptide synthesis as a building block, where the benzyl group serves as a protecting group for the hydroxyl group, preventing unwanted side reactions during the synthesis process. The protecting group can be removed under specific conditions to yield the desired peptide sequence. H-Gly-Ser-OBzl plays a crucial role in the development of pharmaceuticals, bioactive peptides, and other peptide-based compounds, showcasing its importance in the field of organic chemistry and biochemistry.

1738-97-2

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1738-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1738-97-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,3 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1738-97:
(6*1)+(5*7)+(4*3)+(3*8)+(2*9)+(1*7)=102
102 % 10 = 2
So 1738-97-2 is a valid CAS Registry Number.

1738-97-2Downstream Products

1738-97-2Relevant academic research and scientific papers

THE USE OF PENICILLIN ACYLASE FOR SELECTIVE N-TERMINAL DEPROTECTION IN PEPTIDE SYNTHESIS

Waldmann, Herbert

, p. 1131 - 1134 (2007/10/02)

Penicillin acylase from E. coli (EC 3.5.1.11) accepts a broad range of N-phenylacetyl-dipeptide esters as substrates.The enzyme hydrolyses the N-terminal protecting group selectively at room temp. and pH=8.1 without affecting the peptide- or the ester-bonds.Alternatively methyl-, benzyl-, tert-butyl and allyl esters can be cleaved chemically leaving the phenylacetamido moiety intact.

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