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Monopropyl carbonotrithioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68060-07-1

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68060-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68060-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,6 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68060-07:
(7*6)+(6*8)+(5*0)+(4*6)+(3*0)+(2*0)+(1*7)=121
121 % 10 = 1
So 68060-07-1 is a valid CAS Registry Number.

68060-07-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name propylsulfanylmethanedithioate

1.2 Other means of identification

Product number -
Other names Propyl-trithiokohlensaeure

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:68060-07-1 SDS

68060-07-1Downstream Products

68060-07-1Relevant academic research and scientific papers

Development of a practical and convergent process for the preparation of sulopenem

Brenek, Steven J.,Caron, Stephane,Chisowa, Esmort,Delude, Mark P.,Drexler, Michele T.,Ewing, Marcus D.,Handfield, Robert E.,Ide, Nathan D.,Nadkarni, Durgesh V.,Nelson, Jade D.,Olivier, Mark,Perfect, Hahdi H.,Phillips, James E.,Teixeira, John J.,Weekly, R. Matt,Zelina, John P.

, p. 1348 - 1359 (2012/10/29)

Previous synthetic processes for the preparation of sulopenem involved multistep linear sequences in which the chiral sulfoxide side chain was introduced early in the process. This contribution summarizes the development of a practical and convergent process for the large-scale preparation of 1. The key step in the synthesis involves cyclization of an oxalimide intermediate to provide the thiopenem core. This convergent strategy allows for late introduction of the expensive and labile chiral sulfoxide subunit. Additionally, a regioselective sulfur oxidation and an improved deprotection sequence were developed. The latter provides API of high purity without the need for recrystallization.

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