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116143-05-6

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116143-05-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116143-05-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,4 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116143-05:
(8*1)+(7*1)+(6*6)+(5*1)+(4*4)+(3*3)+(2*0)+(1*5)=86
86 % 10 = 6
So 116143-05-6 is a valid CAS Registry Number.

116143-05-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name allo-1-(4-tolylsulfonyl)-4-[[(4-methylphenyl)sulfonyl]oxy]-D-proline ethyl ester

1.2 Other means of identification

Product number -
Other names allo-1-(4-Tolylsulfonyl)-4-((4-tolylsulfonyl)oxy)-D-proline Ethyl Ester

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:116143-05-6 SDS

116143-05-6Relevant articles and documents

FUSED PYRAZINE COMPOUNDS USEFUL FOR THE TREATMENT OF DEGENERATIVE AND INFLAMMATORY DISEASES

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Page/Page column 35, (2009/12/05)

Novel[1.2.4]triazolo[1,5-a]pyrazine and imidazo[1,2-a]pyrazine compounds are disclosed that have a formula represented by the following: The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, pain, inflammation, and others.

Azadideoxyadenosine: Synthesis, enzymology, and anti-HIV activity

Nishonov, Abdumalik A.,Ma, Xiaohui,Nair, Vasu

, p. 4099 - 4101 (2007/10/03)

Synthesis of an azanucleoside, a new analogue of dideoxyadenosine, is described. This compound is only slowly deaminated by mammalian adenosine deaminase and it is a substrate for adenosine kinase. It exhibits in vitro anti-HIV activity.

Synthesis of (S,S)- and (R,R)-2-Alkyl-2,5-diazabicycloheptanes

Braish, Tamim F.,Fox, Darell E.

, p. 1684 - 1687 (2007/10/02)

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