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(4-tert-butylphenyl)(chloro)oxophosphonium, also known as tert-butylphenyl chloro(benzylidene)oxophosphonium, is a phosphonium compound characterized by its molecular formula C15H18ClO2P. It is distinguished by its highly reactive oxophosphonium group, which is instrumental in its various applications.

75213-02-4

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75213-02-4 Usage

Uses

Used in Organic Synthesis:
(4-tert-butylphenyl)(chloro)oxophosphonium is used as a catalyst and reagent for the formation of carbon-carbon and carbon-heteroatom bonds, which are crucial in creating complex molecular structures.
Used in Pharmaceutical Production:
(4-tert-butylphenyl)(chloro)oxophosphonium is utilized as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicines.
Used in Agrochemical Production:
(4-tert-butylphenyl)(chloro)oxophosphonium is also employed in the production of agrochemicals, playing a significant role in the creation of substances that protect crops and enhance agricultural productivity.
Used in Material Science:
Its reactivity and stability make (4-tert-butylphenyl)(chloro)oxophosphonium an important tool in the field of synthetic chemistry, particularly for the development of new materials with specific properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 75213-02-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,1 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 75213-02:
(7*7)+(6*5)+(5*2)+(4*1)+(3*3)+(2*0)+(1*2)=104
104 % 10 = 4
So 75213-02-4 is a valid CAS Registry Number.

75213-02-4SDS

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 (tert-Butyl)phenylphosphinic chloride

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:75213-02-4 SDS

75213-02-4Relevant articles and documents

Unexpected conversions of selected heteroorganic compounds

Drabowicz, Jozef

, p. 437 - 442 (2007/10/03)

A few unexpected conversions of selected heteroorganic compounds are described, including the formation of N-sulfonyl sulfenamide derivatives and the mixed phosphinyl-sulfenyl anhydrides in the reactions of sulfinyl chlorides with α-phenylethylamine or t-butyl-phenylphosphine oxide, respectively. Unexpected reactions of the ortho hydroxyalkyl-substituted diaryl sulfoxides and hypervalent sulfur and selenium derivatives, induced by triphenylphosphine, are also presented. Attempts to rationalize the observed reaction courses are briefly discussed.

Srereoselective Synthesis and Stereochemistry of Optically Active tert-Butylphenylphosphine Sulfide

Skrzypczynski, Zbigniew,Michalski, Jan

, p. 4549 - 4551 (2007/10/02)

Stereoselective reduction of the mixed anhydride of tert-butylphenylphosphinothioic acid trifluoromethanesulfonic acid by sodium borohydride provides optically active tert-butylphenylphosphine sulfide of high optical purity.A synthesis of optically active

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