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Diisopropyl chlorophosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2574-25-6

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2574-25-6 Usage

Chemical Properties

Clear Colourless Liquid

Uses

A phosphorylating agent

Synthesis Reference(s)

Synthetic Communications, 23, p. 1771, 1993 DOI: 10.1080/00397919308011275

Check Digit Verification of cas no

The CAS Registry Mumber 2574-25-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,7 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2574-25:
(6*2)+(5*5)+(4*7)+(3*4)+(2*2)+(1*5)=86
86 % 10 = 6
So 2574-25-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H14ClO3P/c1-5(2)9-11(7,8)10-6(3)4/h5-6H,1-4H3

2574-25-6 Well-known Company Product Price

  • Brand
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  • CAS number
  • Packaging
  • Price
  • Detail

  • Aldrich

  • (672114)  Diisopropylchlorophosphate  97%

  • 2574-25-6

  • 672114-1G

  • 735.93CNY

  • Detail

  • Aldrich

  • (672114)  Diisopropylchlorophosphate  97%

  • 2574-25-6

  • 672114-5G

  • 2,893.41CNY

  • Detail

2574-25-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Diisopropyl Phosphorochloridate

1.2 Other means of identification

Product number -
Other names Diisopropyl phosphorochloridate

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:2574-25-6 SDS

2574-25-6Relevant academic research and scientific papers

Reactions of Phosphorylsulfenyl Chlorides with 2H-1,2,3-Diazaphospholes

Khusainova,Zyablikova,Reshetkova,Lamm,Cherkasov

, p. 1411 - 1413 (2007/10/03)

Formation of a quasiphosphonium salt in reaction of phosphorylsulfenyl chlorides with 1,2,3-diazaphospholes was established by dynamic 31P NMR spectroscopy. The salt is formed by addition of 2 mol of phosphorylsulfenyl chloride to the σ2λ3P=C endocyclic fragment by the 1,1- and 1,2-addition schemes. Decomposition of the salt yields mainly O,O-dialkyl phosphothiochloridate and, to a lesser extent, dialkyl phosphochloridate.

REACTIONS OF PHOSPHITES WITH TRICHLOROACETONITRILE

Kutyrev, A. A.,Moskva, V. V.,Alparova, M. V.

, p. 1332 - 1336 (2007/10/02)

Dialkyl hydrogen, sodium dialkyl, and dialkyl silyl phosphites react with trichloroacetonitrile by the Atherton-Todd scheme.Trialkyl phosphites add at the C(*)N bond of trichloroacetonitrile with the formation of trialkyl phosphorimidates.

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