217633-72-2 Usage
Properties
Chemical compound
Belongs to the class of organic compounds known as N-acyl-alpha amino acids and derivatives
Derivative of benzylamine and 2-aminomethanesulfonic acid
Commonly used as a pharmaceutical intermediate
Potential building block in synthesis of various pharmaceutical compounds
Used in organic synthesis
Can be modified to create new compounds with potential biological activity
Studied for its potential role in inhibiting certain enzymes
Used as an ingredient in molecular biology and biochemistry research
Specific content
N-acyl-alpha amino acid derivative
Made from benzylamine and 2-aminomethanesulfonic acid
Commonly used in pharmaceutical industry
Potential for creating new pharmaceutical compounds
Potential enzyme inhibitor
Used in molecular biology and biochemistry research
Check Digit Verification of cas no
The CAS Registry Mumber 217633-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,6,3 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 217633-72:
(8*2)+(7*1)+(6*7)+(5*6)+(4*3)+(3*3)+(2*7)+(1*2)=132
132 % 10 = 2
So 217633-72-2 is a valid CAS Registry Number.
217633-72-2Relevant articles and documents
DIPEPTIDYL PEPTIDASE INHIBITORS
-
Page 71, (2010/02/09)
Pharmaceuticals, kits and methods are provided for use with DPP-IV and other S9 proteases that comprise a compound with the formula: (I) where the labeled substituents are as described herein.
Synthesis of cyclic peptidosulfonamides by ring-closing metathesis
Brouwer, Arwin J.,Liskamp, Rob M. J.
, p. 3662 - 3668 (2007/10/03)
N-Protected β-aminoethanesulfonyl chlorides (2a-e) were used in the preparation of sulfonamides 4, 8, 11a-c, and 15. Ring-closing metathesis of sulfonamides 4 and 8 did not lead to the expected nine-membered cyclic peptidosulfonamides. In contrast, the al
