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1,3-Dithiol-2-one,4-(1-methylethyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73872-22-7

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73872-22-7 Usage

Type of compound

Dithiolone derivative

Structural feature

Branched isopropyl group attached to the fourth carbon atom

Usage

Primarily used in organic synthesis and medicinal chemistry

Potential applications

Development of pharmaceuticals, building block for complex organic molecules

Importance

Intermediate in the production of pharmaceuticals and agrochemicals

Field of relevance

Chemical research and development

Check Digit Verification of cas no

The CAS Registry Mumber 73872-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,7 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73872-22:
(7*7)+(6*3)+(5*8)+(4*7)+(3*2)+(2*2)+(1*2)=147
147 % 10 = 7
So 73872-22-7 is a valid CAS Registry Number.

73872-22-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-isopropyl-1,3-dithiol-2-one

1.2 Other means of identification

Product number -
Other names 4-Isopropyl-[1,3]dithiol-2-one

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:73872-22-7 SDS

73872-22-7Downstream Products

73872-22-7Relevant academic research and scientific papers

Facile Syntheses of 1,3-Dithiol-2-ones and 1,3-Dithiole-2-thiones

Haley, Neil F.,Fichtner, Michael W.

, p. 2959 - 2962 (2007/10/02)

A facile ring closure of allyl xanthates or trithiocarbonates with iodine is discussed.The products of the reaction undergo basic dehydroiodination and acidic isomerization to give 1,3-dithiol-2-ones and -2-thiones in high yield.

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