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1,3-dithiole 2-tripenylphosphonium hexafluorophosphanate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107907-49-3

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107907-49-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107907-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,9,0 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 107907-49:
(8*1)+(7*0)+(6*7)+(5*9)+(4*0)+(3*7)+(2*4)+(1*9)=133
133 % 10 = 3
So 107907-49-3 is a valid CAS Registry Number.

107907-49-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dithiole 2-tripenylphosphonium hexafluorophosphanate

1.2 Other means of identification

Product number -
Other names -

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:107907-49-3 SDS

107907-49-3Relevant academic research and scientific papers

Synthesis of unsimmetrically substituted tetrathiafulvalenes by the "ylid route". Investigations of selectivity.

Fabre, J. M.,Giral, L.,Gouasmia, A.,Cristau, H. J.,Ribeill, Y.

, p. 823 - 826 (2007/10/02)

The selective synthesis of unsimmetrically substituted tetrathiafulvalenes 1 (R R') using phosphonium ylids 2 and dithiolium salts 3 in THF at -80 deg C has been investigated.Several unsymmetrical tetrathiafulvalenes were obtained in good yield. R,R'=CH3; (CH2)4; o-C6H4.It was also shown that the instability of the phosphonium ylid 2 and dithiolylium 3 under the rreaction conditions leads to the formation of variable amounts of symmetrical terathiafulvalenes 1 (R = R').Therefore, purification of the mixture by column chromatography with CS2 as eluent was necessary.

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