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113397-46-9

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113397-46-9 Usage

Properties

1. Chemical compound belonging to the class of azetidinones
2. Chiral compound
3. Contains a four-membered ring
4. Hydroxyl group attached to the nitrogen atom
5. Methyl group attached to the nitrogen atom
6. Phenylmethyl substituent on the nitrogen atom
7. Potential applications in the pharmaceutical industry

Specific content

1. Belongs to the class of azetidinones
2. Chiral compound with potential pharmaceutical applications
3. Contains a four-membered ring with a hydroxyl group and a methyl group attached to the nitrogen atom
4. Phenylmethyl substituent on the nitrogen atom
5. Potential use in the synthesis of pharmaceuticals and biologically active molecules
6. Important target for research in medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 113397-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,9 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 113397-46:
(8*1)+(7*1)+(6*3)+(5*3)+(4*9)+(3*7)+(2*4)+(1*6)=119
119 % 10 = 9
So 113397-46-9 is a valid CAS Registry Number.

113397-46-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-3-hydroxy-3-methylazetidin-2-one

1.2 Other means of identification

Product number -
Other names 2-Azetidinone,3-hydroxy-3-methyl-1-(phenylmethyl)

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:113397-46-9 SDS

113397-46-9Relevant articles and documents

SOLID STATE PHOTOREACTION OF N,N-DIALKYLPYRUVAMIDES: INCLUSION COMPLEXES WITH DEOXYCHOLIC ACID OR CYCLODEXTRIN

Aoyama, Hiromu,Miyazaki, Ken-ichi,Sakamoto, Masami,Omote, Yoshimori

, p. 1513 - 1518 (2007/10/02)

Solid state photolysis of inclusion molecular complexes of N,N-dialkylpyruvamides with deoxycholic acid or cyclodextrin gave the corresponding β-lactams as main products.The chemo-, stereo-, and regioselectivities of the solid state reactions were different from those of the reactions in solution.Asymmetric induction due to the chirality of deoxycholic acid or cyclodextrin was observed.

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