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2-Pyrrolidinone, 3-methyl-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27948-40-9

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27948-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27948-40-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,4 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27948-40:
(7*2)+(6*7)+(5*9)+(4*4)+(3*8)+(2*4)+(1*0)=149
149 % 10 = 9
So 27948-40-9 is a valid CAS Registry Number.

27948-40-9SDS

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 (3R)-3-Methyl-2-pyrrolidinone

1.2 Other means of identification

Product number -
Other names D-3-METHYLPHENYLALANINE

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:27948-40-9 SDS

27948-40-9Upstream product

27948-40-9Relevant academic research and scientific papers

Separation of (S)-(-)-3-methyl-2-pyrrolidinone as an inclusion complex with (R)-(+)-4,4′,6,6′-tetrachloro-2,2′-bis(hydroxydiphenylmethyl) -1,1′-biphenyl host and its X-ray structural study

Le Roex, Tanya,Nassimbeni, Luigi R.,Toda, Fumio

, p. 77 - 79 (2008/09/19)

By inclusion complexation with the chiral host compound (R)-(+)-4,4′,6,6′-tetrachloro-2,2′-bis(hydroxydiphenylmethyl) -1,1′-biphenyl, racemic 3-methyl-2-pyrrolidinone was resolved and its (S)-(-)-enantiomer was isolated as a 1:1 inclusion complex, which crystallises in the orthorhombic crystal system in the space group P212 121 (a = 14.1163(2) A, b = 14.7140(3) A, c = 17.2025(3) A). By the inclusion complexation, the keto-enol equilibrium of the guest was frozen and the keto-form was isolated in a pure form. By X-ray structural study of the complex, the guest molecule included was elucidated to be the keto-form and its absolute configuration was determined to be (S).

Optical resolution of cyclic amides by inclusion in dehydrocholic acid

Bortolini, Olga,Fogagnolo, Marco,Fantin, Giancarlo,Medici, Alessandro

, p. 206 - 207 (2007/10/03)

Dehydrocholic acid serves as an effective chiral host for the resolution of several five-, six-, and seven-membered cyclic amides by inclusion.

Asymmetric synthesis of 3-substituted pyrrolidones via α-alkylation of a chiral non-racemic γ-lactam

Baussanne, Isabelle,Travers, Catherine,Royer, Jacques

, p. 797 - 804 (2007/10/03)

3-Alkyl pyrrolidones 9 were synthesized in good yield and high diastereoselectivity by α-alkylation of the new chiral non-racemic lactam 8 derived from (R)-(-)-phenylglycinol. After debenzylation and introduction of an electron-withdrawing group, 3-methylpyrrolidone 10 is easily hydrolyzed in a basic medium to produce γ-aminobutyric acid (GABA) analogue 13.

Optically Active 4,4',6,6'-Tetrachloro-2,2'-bis(hydroxydiphenylmethyl)biphenyl As a Host for Optical Resolution and Chiral Shift Reagent

Toda, Fumio,Toyotaka, Ritsuji,Fukuda, Hideji

, p. 303 - 306 (2007/10/02)

The title biphenyl derivative was found to be useful as a host for optical resolution and as a chiral shift reagent for the determination of the optical purity and the absolute configuration of a wide variety of chiral compounds.

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