116339-45-8 Usage
General Description
"2-(3-(tert-butoxycarbonylamino)-2-oxopyrrolidin-1-yl)acetic acid" is a chemical compound with the molecular formula C13H21NO6. It is a derivative of pyrrolidine and contains a tert-butoxycarbonyl (Boc) protecting group. 2-(3-(TERT-BUTOXYCARBONYLAMINO)-2-OXOPYRROLIDIN-1-YL)ACETICACID is commonly used in the synthesis of pharmaceuticals and as a building block for various organic compounds. It has potential applications in the development of drug delivery systems and as a tool in organic chemistry research. Its precise applications and properties depend on the specific context and intended use in chemical synthesis or other applications.
Check Digit Verification of cas no
The CAS Registry Mumber 116339-45-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,3,3 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116339-45:
(8*1)+(7*1)+(6*6)+(5*3)+(4*3)+(3*9)+(2*4)+(1*5)=118
118 % 10 = 8
So 116339-45-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H18N2O5/c1-11(2,3)18-10(17)12-7-4-5-13(9(7)16)6-8(14)15/h7H,4-6H2,1-3H3,(H,12,17)(H,14,15)
116339-45-8Relevant articles and documents
3-AMINO-2-OXO-1-PIPERIDINEACETIC DERIVATIVES CONTAINING AN ARGININE MIMIC AS ENZYME INHIBITORS
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, (2008/06/13)
The present invention discloses peptide aldehydes having a lactam group as part of the peptide backbone and having an original mimic group such as an amidinopiperidine or amidinophengyl tail. These compounds are potent and specific inhibitors of thrombin,
3-amino-2-oxo-1-piperidineacetic derivatives as enzyme inhibitors
-
, (2008/06/13)
The present invention discloses peptide aldehydes which are potent and specific inhibitors of thrombin, their pharmaceutically acceptable salts, pharmaceutically acceptable compositions thereof, and methods of using them as therapeutic agents for disease
Dopamine Receptor Modulation by Conformationally Constrained Analogues of Pro-Leu-Gly-NH2
Yu, Kuo-Long,Rajakumar, G.,Srivastava, Lalit K.,Mishra, Ram K.,Johnson, Rodney L.
, p. 1430 - 1436 (2007/10/02)
Two series of conformationally constrained analogues of Pro-Leu-Gly-NH2 (PLG) have been synthesized.In one series of analogues, the Leu-Gly-NH2 dipeptide segment of PLG was replaced with the γ-lactam residues 3(S)- and 3(R)-amino-2-oxopyrrolidineacetamide
