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2-Azetidinone, 1-[(1,1-dimethylethyl)dimethylsilyl]-3-ethyl-4-(phenylthio)-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79759-95-8

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79759-95-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79759-95-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,5 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79759-95:
(7*7)+(6*9)+(5*7)+(4*5)+(3*9)+(2*9)+(1*5)=208
208 % 10 = 8
So 79759-95-8 is a valid CAS Registry Number.

79759-95-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S*,4R*)-N-(tert-butyldimethylsilyl)-3-ethyl-4-(phenylthio)azetidin-2-one

1.2 Other means of identification

Product number -
Other names 3,4-trans-1-(tert-butyldimethylsilyl)-3-ethyl-4-phenylthio-2-azetidinone

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:79759-95-8 SDS

79759-95-8Relevant academic research and scientific papers

Chemistry of O-silylated ketene acetals: A stereoselective synthesis of optically active carbapenem antibiotics, (+)-thienamycin and (+)-PS-5

Kita,Shibata,Miki,Takemura,Tamura

, p. 12 - 20 (2007/10/02)

A stereoselective synthesis of the chiral thienamycin intermediate (16) involving a diastereoselective Michael addition and a silicon-induced Pummerer-type reaction is described. In a similar way, the key intermediate for (+)-PS-5 was also prepared from 4

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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