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L-α-Benzyloxycarbonylamino-β-benzylthio-propionitril is a complex organic compound with the molecular formula C20H20N2O2S. It is a derivative of propionitril, featuring a benzyloxycarbonyl (Cbz) group attached to the α-amino position and a benzylthio group at the β-position. L-α-Benzyloxycarbonylamino-β-benzylthio-propionitril is often used in peptide synthesis as a protecting group for amino acids, particularly in solid-phase peptide synthesis. The benzyloxycarbonyl group serves to protect the amino group, while the benzylthio group protects the carboxylic acid group, allowing for selective reactions and purification steps during peptide assembly. The compound's structure and protective groups are crucial for controlling the reactivity and selectivity of the amino acid during peptide bond formation, ultimately leading to the desired peptide sequence.

3589-40-0

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3589-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3589-40-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,8 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3589-40:
(6*3)+(5*5)+(4*8)+(3*9)+(2*4)+(1*0)=110
110 % 10 = 0
So 3589-40-0 is a valid CAS Registry Number.

3589-40-0Downstream Products

3589-40-0Relevant academic research and scientific papers

One-pot synthesis of orthogonally protected dipeptide selenazoles employing Nα-amino selenocarboxamides and α-bromomethyl ketones

Madhu, Chilakapati,Panguluri, Nageswara Rao,Narendra,Panduranga,Sureshbabu, Vommina V.

, p. 6831 - 6835 (2014)

A simple and efficient protocol for the synthesis of selenazole containing dipeptidomimetics using Nα-amino selenocarboxamides and α-bromomethyl ketones is described. All the compounds made were isolated in good yields and fully characterized.

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