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3285-53-8

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3285-53-8 Usage

General Description

9H-Thioxanthene-2-sulfonamide, N,N-dimethyl-9-oxo- is a chemical compound that belongs to the thioxanthene class. It is a sulfonamide derivative of thioxanthene, featuring a sulfonamide group at the 2-position and a dimethylcarbamoyl group at the 9-position. 9H-Thioxanthene-2-sulfonamide, N,N-dimethyl-9-oxo- has potential pharmacological activity as it is a derivative of thioxanthene, which is known for its antipsychotic and antihistaminic properties. Additionally, the presence of the dimethylcarbamoyl group suggests potential activity as a drug candidate. Further research and studies are needed to fully understand the properties and potential applications of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 3285-53-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,8 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3285-53:
(6*3)+(5*2)+(4*8)+(3*5)+(2*5)+(1*3)=88
88 % 10 = 8
So 3285-53-8 is a valid CAS Registry Number.

3285-53-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(N,N-dimethylsulphonamido)thioxanthen-9-one

1.2 Other means of identification

Product number -
Other names 2-N,N-Dimethylsulfonamidothioxanthone

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:3285-53-8 SDS

3285-53-8Upstream product

3285-53-8Relevant articles and documents

Chemical and photooxidation of thiothixene (Navane): structure of the thiothixene fluorophor

Eiden,Ruth

, p. 1062 - 1063 (1978)

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