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188530-96-3

Propanoic acid, 3-[[(4-nitrophenyl)sulfonyl]oxy]-2-oxo-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

188530-96-3

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188530-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 188530-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,5,3 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 188530-96:
(8*1)+(7*8)+(6*8)+(5*5)+(4*3)+(3*0)+(2*9)+(1*6)=173
173 % 10 = 3
So 188530-96-3 is a valid CAS Registry Number.

188530-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-(4-nitrophenyl)sulfonyloxy-2-oxopropanoate

1.2 Other means of identification

Product number -
Other names -

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:188530-96-3 SDS

188530-96-3Relevant articles and documents

COMPOUNDS TO TREAT AMYLOIDOSIS AND PREVENT DEATH OF BETA-CELLS IN TYPE 2 DIABETES MELLITUS

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Page/Page column 52, (2010/11/24)

The invention discloses aromatic amides and sulfonates to treat or prevent type 2 diabetes mellitus (T2DM), the pathological consequences of T2DM, to inhibit amyloidosis or to prevent death of β-cells of the pancreas.

Synthesis and Reactions of 3-(Nosyloxy)-2-keto Esters

Hoffman, Robert V.,Catherine Johnson,Okonya, John F.

, p. 2458 - 2465 (2007/10/03)

A series of 3-(nosyloxy)-2-keto esters 7a-j were prepared from the corresponding α-keto esters by conversion to the trimethylsilyl enol ether and reaction with p-nitrobenzenesulfonyl peroxide. Conversion of these materials to 1,2,3-trifunctionalized compounds is described, and comparison of their properties with isomeric 2-(nosyloxy)-3-keto esters is discussed.

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