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24463-84-1

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24463-84-1 Usage

General Description

The chemical "(1,1-dioxidotetrahydrothiophen-2-yl)(phenyl)methanone" is a compound with the molecular formula C13H11NO3S. It consists of a tetrahydrothiophene ring with a ketone group and a phenyl group attached to it. (1,1-dioxidotetrahydrothiophen-2-yl)(phenyl)methanone has potential applications in pharmaceuticals, agrochemicals, and materials science due to its diverse reactivity and functional groups. Additionally, its aromatic nature and potential for hydrogen bonding suggest it may have interesting biological and pharmacological properties. However, further research and testing are required to fully understand the properties and potential uses of "(1,1-dioxidotetrahydrothiophen-2-yl)(phenyl)methanone" in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 24463-84-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,6 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24463-84:
(7*2)+(6*4)+(5*4)+(4*6)+(3*3)+(2*8)+(1*4)=111
111 % 10 = 1
So 24463-84-1 is a valid CAS Registry Number.

24463-84-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (1,1-dioxothiolan-2-yl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names 1,1-Dioxy-2-thiolanyl-phenyl-keton

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:24463-84-1 SDS

24463-84-1Downstream Products

24463-84-1Relevant articles and documents

Efficient conversion of sulfones into β-keto sulfones by N-acylbenzotriazoles

Katritzky, Alan R.,Abdel-Fattah, Ashraf A. A.,Wang, Mingyi

, p. 1443 - 1446 (2007/10/03)

Acyclic sulfones 4a-f and alicyclic sulfone 7 react with readily available N-acylbenzotriazoles 3a-g (derived from aliphatic, aromatic, and heteroaromatic carboxylic acids) to provide the corresponding β-keto sulfones 5a-n and 8a-c, respectively, in good

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