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2-chloroethyl diphenylphosphinate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92982-05-3

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92982-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92982-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,8 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92982-05:
(7*9)+(6*2)+(5*9)+(4*8)+(3*2)+(2*0)+(1*5)=163
163 % 10 = 3
So 92982-05-3 is a valid CAS Registry Number.

92982-05-3SDS

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 [2-chloroethoxy(phenyl)phosphoryl]benzene

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:92982-05-3 SDS

92982-05-3Downstream Products

92982-05-3Relevant academic research and scientific papers

A solvent-free method for the preparation of phosphinates from P(O)-OH compounds with alkyl chlorides

Yuan, Huihui,Wang, Mingyue,Fan, Lei,Yang, Jia,Wang, Shuai,Zhong, Hong

supporting information, (2021/11/17)

Herein, a new solvent-free synthetic method using P(O)-OH compound and alkyl chloride for phosphinate compounds is disclosed. This transformation proceeds smoothly under the promotion of a lone base and presents the advantages of an easily available raw material source, a simple post treatment process, good functional group tolerance and high reaction efficiency. Good yield was obtained when the reaction was magnified to gram scale, and the molar ratio of P(O)-OH compounds and alkyl chlorides can be decreased to 1:2. This protocol provides a practical method for the preparation of phosphorus derivatives. Furthermore, the reaction mechanism was explored by means of 31P NMR.

Synthesis of phosphorus derivatives from 1,3-dioxolan-2-one

Ilia, Gheorghe,Bora, Alina,Iliescu, Smaranda,Popa, Adriana,Dehelean, Gheorghe

, p. 2491 - 2496 (2007/10/03)

A new route for the synthesis of some mixed organic phosphorus compounds from 1,3-dioxolan-2-one is reported. By heating a mixture of phosphorus-chlorine derivatives and 1,3-dioxolan-2-one in the presence of a catalyst, mixed phosphorus derivatives having 2-chloroethyl ester groups could be obtained. A wide range of phosphorus derivatives can be obtained using this method.

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