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1498-46-0

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1498-46-0 Usage

Description

ISOPROPYL PHOSPHONIC DICHLORIDE is an organic compound with the chemical formula (CH3)2CHOP(O)Cl2. It is a colorless to pale yellow liquid and is used as a chemical intermediate in the synthesis of various compounds.

Uses

Used in Chemical Synthesis:
ISOPROPYL PHOSPHONIC DICHLORIDE is used as a chemical intermediate for the preparation of bis(fluoroalkyl) alkylphosphonates. It reacts with fluoroalcohols in the presence of triethylamine as a catalyst, which is crucial for the formation of these specific phosphonate compounds.
Used in Pharmaceutical Industry:
ISOPROPYL PHOSPHONIC DICHLORIDE is used as a building block in the synthesis of various pharmaceutical compounds. Its reactivity and versatility make it a valuable component in the development of new drugs and therapeutic agents.
Used in Material Science:
In the field of material science, ISOPROPYL PHOSPHONIC DICHLORIDE is utilized as a precursor for the development of novel materials with specific properties, such as improved thermal stability or enhanced chemical resistance.
Used in Agrochemical Industry:
ISOPROPYL PHOSPHONIC DICHLORIDE is employed as a starting material for the synthesis of various agrochemicals, including pesticides and herbicides. Its role in these applications is to provide a stable and effective active ingredient for controlling pests and weeds in agricultural settings.

Check Digit Verification of cas no

The CAS Registry Mumber 1498-46-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,9 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1498-46:
(6*1)+(5*4)+(4*9)+(3*8)+(2*4)+(1*6)=100
100 % 10 = 0
So 1498-46-0 is a valid CAS Registry Number.
InChI:InChI=1/C3H7Cl2OP/c1-3(2)7(4,5)6/h3H,1-2H3

1498-46-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H27109)  Isopropylphosphonic dichloride, tech. 90%   

  • 1498-46-0

  • 1g

  • 412.0CNY

  • Detail
  • Alfa Aesar

  • (H27109)  Isopropylphosphonic dichloride, tech. 90%   

  • 1498-46-0

  • 5g

  • 1264.0CNY

  • Detail

1498-46-0SDS

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-dichlorophosphorylpropane

1.2 Other means of identification

Product number -
Other names isopropylphosphonyl 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:1498-46-0 SDS

1498-46-0Relevant articles and documents

A novel and efficient synthesis of N,N-dialkylaminoisopropyl- and O-alkylisopropyl-2-(1-alkyl-2-oxopropylidene)phosphonohydrazido oximes - Potential marine fish toxin analogues. Part 1

Kumar, Rajesh,Gupta, Arvind K.,Kaushik, Mahabir P.

, p. 1334 - 1340 (2007)

A novel and efficient method for the synthesis of N,N- dialkylaminoisopropyland O-alkylisopropyl-2-(1-alkyl-2-oxopropylidene) phosphonohydrazido oximes (4) using activated silica as dehydrating agent has been developed. The reaction involves the condensat

Easy preparation of alkylphosphonyl dichlorides

Patois, C.,Berte-Verrando, S.,Savignac, P.

, p. 485 - 487 (2007/10/02)

Phosphonic acid esters bearing an alkyl, halogen or carboxylate substituent on the α-carbon are readily converted into the parent phosphonic dichlorides when treated with a mixture of 2.5 eq of phosphorus pentachloride and 1.3 eq of phosphorus oxychloride.Keywords - phosphonates / chlorination / phosphorus pentachloride / phosphorus oxychloride / phosphonyl dichloride

REDUCTION OF CHLOROPHOSPHONIUM COMPOUNDS BY COMPOUNDS OF PIII AS A HALOPHILIC REACTION

Timokhin, B. V.,Vengel'nikova, V. N.,Kalabina, A. V.,Donskikh, V. I.

, p. 1307 - 1310 (2007/10/02)

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