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4-Phenyl-3H-1,2-dithiol-3-one is an organic compound with the chemical formula C8H6OS2. It is a derivative of 1,2-dithiol-3-one, featuring a phenyl group attached to the 4-position. This molecule is characterized by the presence of a 3H-1,2-dithiol-3-one core, which consists of a sulfur atom double-bonded to a carbonyl group (C=O) and another sulfur atom single-bonded to the same carbonyl carbon. The phenyl ring provides additional stability and reactivity to the molecule. 4-Phenyl-3H-1,2-dithiol-3-one is known for its unique chemical properties and potential applications in various fields, such as pharmaceuticals and materials science. It is important to note that handling and storage of 4-Phenyl-3H-1,2-dithiol-3-one should be done with caution, as it may have specific safety and stability requirements.

3467-32-1

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3467-32-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3467-32-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,6 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3467-32:
(6*3)+(5*4)+(4*6)+(3*7)+(2*3)+(1*2)=91
91 % 10 = 1
So 3467-32-1 is a valid CAS Registry Number.

3467-32-1SDS

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 4-Phenyl-1,2-dithiol-3-one

1.2 Other means of identification

Product number -
Other names 4-Phenyl-1,2-dithiolon-(3)

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:3467-32-1 SDS

3467-32-1Upstream product

3467-32-1Relevant academic research and scientific papers

Selective [3 + 2] Cycloaddition of Cyclopropenone Derivatives and Elemental Chalcogens

Wu, Jian,Gao, Wen-Xia,Huang, Xiao-Bo,Zhou, Yun-Bing,Liu, Miao-Chang,Wu, Hua-Yue

supporting information, p. 5555 - 5560 (2020/07/30)

A highly efficient method is disclosed for the synthesis of 1,2-dichalcogen heterocycles via [3 + 2] cycloaddition of cyclopropenone derivatives and elemental chalcogens. Different from other cyclopropenone derivatives, cyclopropenselenones undergo unprec

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