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2032-48-6

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2032-48-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2032-48-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,3 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2032-48:
(6*2)+(5*0)+(4*3)+(3*2)+(2*4)+(1*8)=46
46 % 10 = 6
So 2032-48-6 is a valid CAS Registry Number.

2032-48-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (6Z)-6-[piperidin-1-yl(sulfanyl)methylidene]cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names HMS2186K08

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:2032-48-6 SDS

2032-48-6Relevant articles and documents

Syntheses and antitumor activities of N′1, N′3-dialkyl-N′1,N′3-di- (alkylcarbonothioyl) malonohydrazide: The discovery of elesclomol

Chen, Shoujun,Sun, Lijun,Koya, Keizo,Tatsuta, Noriaki,Xia, Zhiqiang,Korbut, Timothy,Du, Zhenjian,Wu, Jim,Liang, Guiqing,Jiang, Jun,Ono, Mitsunori,Zhou, Dan,Sonderfan, Andrew

, p. 5070 - 5076 (2013/09/12)

A series of N′1,N′3-dialkyl- N′1,N′3-di(alkylcarbonothioyl) malonohydrazides have been designed and synthesized as anticancer agents by targeting oxidative stress and Hsp70 induction. Structure-activity relationship (SAR) studies lead to the discovery of STA-4783 (elesclomol), a novel small molecule that has been evaluated in a number of clinical trials as an anticancer agent in combination with Taxol.

Examinations of thioamides and their derivatives. X. Salts 1-(o-hydroxy)-alpha-alkylthiobenzylidene) piperidinium, structure, properties and biological activity

Santus,Soltysiak,Smolinski,Stefaniak

, p. 189 - 193 (2007/10/02)

In reactions of 1-(o-hydroxy)thiobenzoylpiperidine with alkyl halides there was obtained 1-(o-hydroxy-alpha-alkylthiobenzylidene)piperidinium bromides and iodides. Structure of obtained compounds have been determined by spectroscopic methods. Products of hydrolysis their and antimitotic and enzymatic activity were investigated too.

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