261896-35-9 Usage
Uses
Used in Pharmaceutical Research and Development:
4,4-DIMETHYL-PYRROLIDINE-3-CARBOXYLIC ACID is used as a chemical intermediate for the synthesis of various drugs and organic compounds, contributing to the development of new pharmaceuticals.
Used in Chemical Research:
4,4-DIMETHYL-PYRROLIDINE-3-CARBOXYLIC ACID is used as a research compound to explore its potential pharmacological activities, including its role as an anti-inflammatory and anesthetic agent.
Used in Materials Science:
4,4-DIMETHYL-PYRROLIDINE-3-CARBOXYLIC ACID is used in the development of new materials and polymers due to its unique chemical structure, which may offer novel properties and applications in various industries.
Used in the Development of New Compounds:
4,4-DIMETHYL-PYRROLIDINE-3-CARBOXYLIC ACID is used as a building block in the creation of new organic compounds, potentially leading to advancements in chemical synthesis and the discovery of new chemical entities with specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 261896-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,8,9 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 261896-35:
(8*2)+(7*6)+(6*1)+(5*8)+(4*9)+(3*6)+(2*3)+(1*5)=169
169 % 10 = 9
So 261896-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO2/c1-7(2)4-8-3-5(7)6(9)10/h5,8H,3-4H2,1-2H3,(H,9,10)
261896-35-9Relevant articles and documents
Enantioselective synthesis of gabapentin analogues via organocatalytic asymmetric Michael addition of α-branched aldehydes to β-nitroacrylates
Yoshida, Masanori,Masaki, Erika,Ikehara, Hiroto,Hara, Shoji
experimental part, p. 5289 - 5297 (2012/08/08)
Michael addition reaction of α-branched aldehydes to β-nitroacrylates was successfully carried out by using a mixed catalyst consisting of a primary amino acid, l-phenylalanine, and its lithium salt to give β-formyl-β′-nitroesters having a quaternary carbon centre in good yields (up to 85%) with high enantioselectivity (up to 98% ee). By using benzyl β-nitroacrylates as Michael acceptors, the obtained β-formyl-β′-nitroesters were converted into various 4,4-disubstituted pyrrolidine-3-carboxylic acids including analogues of gabapentin (Neurotin) in one step from the Michael adducts in high yields. The Royal Society of Chemistry 2012.
Branched alkyl pyrrolidine-3-carboxylic acids
-
, (2008/06/13)
Branched alkyl pyrrolidines of formula (I) are disclosed and are useful as agents in the treatment of epilepsy, faintness attacks, hypokinesia, cranial disorders, neurodegenerative disorders, depression, anxiety, panic, pain, and neuropatnological disorders. Processes for the preparation and intermediates useful in the preparation are also disclosed.
