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75032-27-8

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75032-27-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75032-27-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,3 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75032-27:
(7*7)+(6*5)+(5*0)+(4*3)+(3*2)+(2*2)+(1*7)=108
108 % 10 = 8
So 75032-27-8 is a valid CAS Registry Number.

75032-27-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl [(p-nitrophenyl)thio]acetate

1.2 Other means of identification

Product number -
Other names ethyl 2-(4-nitrophenylthio)acetate

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:75032-27-8 SDS

75032-27-8Relevant articles and documents

STRAD-BINDING AGENTS AND USES THEREOF

-

Paragraph 0772-0774, (2021/08/06)

Disclosed herein, inter alia, are compounds for binding STRAD pseudokinase and uses thereof.

Rhodium-Catalyzed Rearrangement of S/Se-Ylides for the Synthesis of Substituted Vinylogous Carbonates

Reddy, Angula Chandra Shekar,Anbarasan, Pazhamalai

supporting information, p. 9965 - 9969 (2019/12/24)

An efficient rhodium-catalyzed unprecedented oxa-[2,3]-sigmatropic rearrangement of sulfur ylide derived from α-thioesters/ketones and diazo carbonyl compounds has been accomplished for the synthesis of various sulfur-tethered vinylogous carbonates in good to excellent yields. Important features of the developed reaction include wide functional group tolerance, excellent chemo- and regioselectivity, and efficient rearrangement involving the carbonyl motif. The present reaction also equally works well with α-selenoesters for the synthesis of seleno-containing vinylogous carbonates.

Synthesis of thioether andrographolide derivatives and their inhibitory effect against cancer cells

Liu, Yi,Liang, Ren-Ming,Ma, Qing-Ping,Xu, Kai,Liang, Xin-Yong,Huang, Wei,Sutton, Robert,Ding, Jie,O'Neil, Paul M.,Cheng, Chun-Ru

, p. 1268 - 1274 (2017/07/07)

A series of novel thioether andrographolide derivatives were synthesized by incorporating various aromatic (or heteroaromatic) substituents into C-12 or 14-OH. A total of 38 andrographolide derivatives were prepared and evaluated for their in vitro inhibi

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