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1,3,2,4-Dithiadiphosphetane, 2,4-dicyclohexyl-, 2,4-disulfide is a complex organic compound with the chemical formula C12H20P2S4. It features a dithiadiphosphetane ring, which consists of two phosphorus atoms bonded to each other, with sulfur atoms attached to the phosphorus atoms, forming a four-membered ring. The compound also has two cyclohexyl groups attached to the phosphorus atoms, which contribute to its stability and reactivity. 1,3,2,4-Dithiadiphosphetane, 2,4-dicyclohexyl-, 2,4-disulfide is known for its unique structure and potential applications in various chemical reactions, such as in the synthesis of phosphorus-containing compounds and as a ligand in coordination chemistry. Due to its complex structure and potential applications, it is of interest to researchers in the field of organic and inorganic chemistry.

1024-06-2

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1024-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1024-06-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1024-06:
(6*1)+(5*0)+(4*2)+(3*4)+(2*0)+(1*6)=32
32 % 10 = 2
So 1024-06-2 is a valid CAS Registry Number.

1024-06-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(cyclohexylphosphonotrithioic) bisthioanhydride

1.2 Other means of identification

Product number -
Other names 2,4-Dicyclohexyl-[1,3,2,4]dithiadiphosphetane 2,4-disulfide

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:1024-06-2 SDS

1024-06-2Relevant academic research and scientific papers

DIE STRUKTUR VON ALKYL- UND ARYLPERTHIOPHOSPHONSAEUREANHYDRIDEN IN LOESUNG

Ohms, Gisela,Treichler, Antje,Grossmann, Gisbert

, p. 95 - 102 (2007/10/02)

The analysis of 1H-, 31P- and 13C-NMR spectra of different alkyl- and arylperthiophosphonic acid anhydrides shows that these compounds prefer a dimeric structure in solution.They exist as 2,4-diorganyl-2,4-dithioxo-1,3,2λ5,4λ5-dithiadiphosphetanes.Most of the perthiophosphonic acid anhydrides form configuration isomers which differ in the position of the thioxo groups relatively to the ring plane.The concentration of the trans-isomer is generally larger than that of the cis-isomer.The ratio of the concentration of both isomers is obviously determined by the polarity of the solvent used.Mixing of solutions of different perthiophosphonic acid anhydrides results in unsymmetrical compounds also existing in cis- and trans-configuration. 31P chemical shifts and geminal P-P coupling constants for symmetrical and unsymmetrical perthiophosphonic acid anhydrides are presented and discussed. - Key words: 31P chemical shifts; P-P coupling constants; perthiophosphonic acid anhydrides; mixed perthiophosphonic acid anhydrides; configuration isomers; 2,4-diorganyl-2,4-dithioxo-1,3,2λ5,4λ5-dithiadiphosphetanes.

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