3005-85-4 Usage
General Description
4-Methyl-2-pyrrolidine carboxylic acid is a chemical compound with the molecular formula C6H11NO2. It is a derivative of pyrrolidine and is a white crystalline powder. 4-METHYL-2-PYRROLIDINE CARBOXYLIC ACID is an amino acid that is not naturally found in the human body but can be synthesized. It has been studied for its potential use in pharmaceuticals and as a building block in organic synthesis. This chemical is known for its ability to act as a chiral auxiliary in asymmetric synthesis and has been explored for its potential application in the creation of pharmaceutical drugs. Additionally, it has also been studied for its potential use in the agricultural industry for the development of crop protection products.
Check Digit Verification of cas no
The CAS Registry Mumber 3005-85-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,0 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3005-85:
(6*3)+(5*0)+(4*0)+(3*5)+(2*8)+(1*5)=54
54 % 10 = 4
So 3005-85-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO2/c1-4-2-5(6(8)9)7-3-4/h4-5,7H,2-3H2,1H3,(H,8,9)
3005-85-4Relevant articles and documents
Revised structure and structure-activity relationship of bisebromoamide and structure of norbisebromoamide from the marine cyanobacterium Lyngbya sp.
Sasaki, Hiroaki,Teruya, Toshiaki,Fukazawa, Hidesuke,Suenaga, Kiyotake
experimental part, p. 990 - 994 (2011/03/19)
Novel potent cytotoxic peptides bisebromoamide (1) and norbisebromoamide (2) have been isolated from the marine cyanobacterium Lyngbya sp. The planar structure of these peptides was elucidated through the extensive application of 1D and 2D NMR techniques. The absolute stereostructure of 1 was determined by chemical degradation followed by chiral HPLC analysis. Recently, Tao and co-workers achieved synthesis of bisebromoamide, and the configuration of thiazoline moiety was revised. We re-investigated the stereochemistry of thiazoline moiety of 1. The structure-activity relationships of bisebromoamide (1) were investigated with the use of natural and synthetic analogs. Furthermore, bisebromoamide (1) potently inhibited protein kinase: the phosphorylation of ERK in NRK cells by PDGF-stimulation was selectively inhibited by treatment with 10-0.1 μM of 1.
