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2-phenyl-1,3,2-dithiaphospholane is a heterocyclic compound characterized by the presence of a phosphorus atom, two sulfur atoms, and a phenyl group. It is a member of the dithiaphospholane family, which are cyclic compounds containing phosphorus and sulfur atoms. The structure of 2-phenyl-1,3,2-dithiaphospholane consists of a phosphorus atom bonded to two sulfur atoms, forming a three-membered ring, with a phenyl group attached to the phosphorus atom. 2-phenyl-1,3,2-dithiaphospholane is of interest in organic chemistry and materials science due to its unique electronic properties and potential applications in the synthesis of various phosphorus-containing compounds.

4669-54-9

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4669-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4669-54-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,6 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4669-54:
(6*4)+(5*6)+(4*6)+(3*9)+(2*5)+(1*4)=119
119 % 10 = 9
So 4669-54-9 is a valid CAS Registry Number.

4669-54-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-1,3,2-dithiaphospholane

1.2 Other means of identification

Product number -
Other names 2-Phenyldithiophospholan

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

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More Details:4669-54-9 SDS

4669-54-9Relevant academic research and scientific papers

General route to phosphonodithioic acid derivatives

Martin,Wagman,Zipp,Gratchev

, p. 7957 - 7958 (2007/10/02)

A general procedure for the synthesis of esters of phosphonodithioic acids has been developed. The method involves the reaction of the Grignard reagents 2a-h with 2-chloro-1,3,2-dithiaphospholane (1) to give 3a-h that were sulfurized using elemental sulfu

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