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Cyclohexylphosphonic dichloride, with the molecular formula C6H11Cl2PO2, is a colorless, liquid chemical compound characterized by a strong odor. It is known for its reactivity with various compounds, making it a versatile reagent in chemical reactions. Due to its potentially hazardous nature, it requires careful handling and appropriate safety measures.

1005-22-7

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1005-22-7 Usage

Uses

Used in Pharmaceutical Industry:
Cyclohexylphosphonic dichloride is used as a reagent for the synthesis of drugs, contributing to the development of new medications and therapeutic agents.
Used in Chemical Industry:
CYCLOHEXYLPHOSPHONIC DICHLORIDE is employed as a reagent in various chemical processes, facilitating the production of different chemical products and intermediates.
Used in Industrial Processes:
Cyclohexylphosphonic dichloride is utilized in industrial applications, where its reactivity plays a crucial role in the manufacturing of various products and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 1005-22-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1005-22:
(6*1)+(5*0)+(4*0)+(3*5)+(2*2)+(1*2)=27
27 % 10 = 7
So 1005-22-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H11Cl2OP/c7-10(8,9)6-4-2-1-3-5-6/h6H,1-5H2

1005-22-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name CYCLOHEXYLPHOSPHONIC DICHLORIDE

1.2 Other means of identification

Product number -
Other names cyclohexylphosphonic acid dichloride

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:1005-22-7 SDS

1005-22-7Relevant academic research and scientific papers

Cyclic Phosphine Oxides and Phosphinamides from Di-Grignard Reagents and Phosphonic Dichlorides: Modular Access to Annulated Phospholanes

Gregson, Aaron M.,Wales, Steven M.,Bailey, Stephen J.,Willis, Anthony C.,Keller, Paul A.

, p. 9774 - 9780 (2015/10/12)

The reaction between 1,4-di-Grignard reagents and phosphonous(III) dichlorides is a classical method for the direct synthesis of phospholanes. Reported here is an extension of this approach to the preparation of value-added, annulated phospholane oxides, achieved through the combination of carbocyclic-fused di-Grignard reagents and readily available phosphonic(V) dichlorides. The procedure is amenable to (benz)annulation at both the 2,3- and 3,4-positions of the phospholane ring, and a variety of aliphatic, cyclic and aryl P-electrophiles are tolerated in reasonable to excellent yields.

Synthesis and NMR study of cyclohexylphosphonates

Titov,Zakharov,Krivchun,Ionin

experimental part, p. 481 - 487 (2011/06/23)

Cyclohexyl-, 2-chlorocyclohex-1-yl and cyclohexen-1-ylphosphonic acids chlorides and fluorides were synthesized and studied by the 1H, 13C, 19F, and 31P NMR methods with the use of correlation spectroscopy and q

A general synthesis of phosphonic acid dichlorides using oxalyl chloride and DMF catalysis

Rogers, Roland S.

, p. 7473 - 7474 (2007/10/02)

A general synthesis of phosphonic diacid dichlorides (1) using oxalyl chloride and catalytic DMF is described.

A MILD AND FACILE SYNTHESIS OF ALKYL- AND ARYLPHOSPHONYL DICHLORIDES UNDER NEUTRAL CONDITIONS. REACTION OF BIS(TRIMETHYLSILYL) PHOSPHONATES WITH PCl5

Morita, Tsuyoshi,Okamoto, Yoshiki,Sakurai, Hiroshi

, p. 435 - 438 (2007/10/02)

Bis(trimethylsilyl) phosphonates, which are prepared from the dialkyl esters with chlorotrimethylsilane/sodium iodide, are transformed in high yields into the corresponding phosphonyl dichlorides on the treatment with phosphorus pentachloride under mild and neutral conditions.

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