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2-Azetidinone, 1-(phenylmethyl)-4-(phenylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138428-96-3

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138428-96-3 Usage

Chemical Structure

2-azetidinone ring
Phenylmethyl group attached
Phenylthio group attached

Utility

Used in the synthesis of various pharmaceutical compounds
Potential biological activities under study

Chemical Properties

Presence of the 2-azetidinone ring
Phenylmethyl group contributes to molecular structure and reactivity
Phenylthio group enhances chemical diversity and potential interactions

Applications

Potential use in drug development
Important building block in organic chemistry synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 138428-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,2 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 138428-96:
(8*1)+(7*3)+(6*8)+(5*4)+(4*2)+(3*8)+(2*9)+(1*6)=153
153 % 10 = 3
So 138428-96-3 is a valid CAS Registry Number.

138428-96-3SDS

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 1-benzyl-4-phenylsulfanylazetidin-2-one

1.2 Other means of identification

Product number -
Other names N-benzyl-4-(phenylthio)azetidin-2-one

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:138428-96-3 SDS

138428-96-3Relevant academic research and scientific papers

Chemistry of O-silylated ketene acetals: A mild and convenient synthesis of β-lactam antibiotics

Kita,Shibata,Tamura,Miki

, p. 2225 - 2232 (2007/10/02)

β-Amido sulfoxides (1) reacted with O-silylated ketene acetal (16) in dry acetonitrile in the presence of a catalytic amount of zinc iodide to give the 4-phenylthioazetidin-2-ones (17). Oxidation of 17 with m-chloroperbenzoic acid gave the corresponding s

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