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113742-94-2

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113742-94-2 Usage

Description

Pyrrolidine, 2-(methoxymethyl)-1-(oxophenylacetyl)-, (S)is a synthetic chirally pure compound belonging to the class of organic chemicals known as beta-lactams. It is characterized by its unique structure, which includes a pyrrolidine ring bonded to a methoxymethyl group and an oxophenylacetyl group. Its asymmetric nature makes it a valuable tool in the manufacture of enantiomerically pure drugs, as well as in the study of chirality in chemical reactions.

Uses

Used in Pharmaceutical Industry:
Pyrrolidine, 2-(methoxymethyl)-1-(oxophenylacetyl)-, (S)is used as a building block in the synthesis of various pharmaceuticals, particularly in the production of cephalosporin antibiotics. Its unique structure and chiral purity make it an essential component in the development of new and improved medications.

Check Digit Verification of cas no

The CAS Registry Mumber 113742-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,7,4 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113742-94:
(8*1)+(7*1)+(6*3)+(5*7)+(4*4)+(3*2)+(2*9)+(1*4)=112
112 % 10 = 2
So 113742-94-2 is a valid CAS Registry Number.

113742-94-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-N-benzoylformyl-2-(methoxymethyl)pyrrolidine

1.2 Other means of identification

Product number -
Other names 1-((S)-2-Methoxymethyl-pyrrolidin-1-yl)-2-phenyl-ethane-1,2-dione

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:113742-94-2 SDS

113742-94-2Relevant articles and documents

Stereocontrolled Addition Reaction of Organometallics to Chiral α-Keto Amides

Fujisawa, Tamotsu,Ukaji, Yutaka,Funabora, Makoto,Yamashita, Mikio,Sato, Toshio

, p. 1894 - 1897 (2007/10/02)

Complementary stereoselection in the addition reaction of several organometallics to chiral benzoylformamide, prepared from benzoylformic acid and (S)-2-(methoxymethyl)pyrrolidine, could be achieved using magnesium- and titanium-based reagents to give different diastereomers of atrolactamide.On the other hand, the reaction of phenyl metallics to the corresponding pyruvamide afforded (S)-atrolactamide.

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