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261896-35-9

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261896-35-9 Usage

General Description

4,4-DIMETHYL-PYRROLIDINE-3-CARBOXYLIC ACID, also known as DMPC, is a chemical compound with the molecular formula C8H15NO2. It is a derivative of pyrrolidone, and it contains a carboxylic acid functional group. DMPC is commonly used in pharmaceutical and chemical research as an intermediate in the synthesis of various drugs and organic compounds. It has been studied for its potential pharmacological activities, including its role as an anti-inflammatory and anesthetic agent. DMPC may also have applications in the development of new materials and polymers due to its unique chemical structure. Overall, DMPC is a valuable compound with diverse uses in the fields of medicine, chemistry, and materials science.

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)

261896-35-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4-dimethylpyrrolidine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4,4-Dimethyl-pyrrolidine-3-carboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:261896-35-9 SDS

261896-35-9Downstream Products

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.

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