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92074-50-5

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92074-50-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92074-50-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,7 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92074-50:
(7*9)+(6*2)+(5*0)+(4*7)+(3*4)+(2*5)+(1*0)=125
125 % 10 = 5
So 92074-50-5 is a valid CAS Registry Number.

92074-50-5SDS

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 [chloro-[chloro(ethoxy)phosphoryl]methyl]benzene

1.2 Other means of identification

Product number -
Other names Ethyl 1-chlorobenzylphosphonochloridate

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:92074-50-5 SDS

92074-50-5Downstream Products

92074-50-5Relevant articles and documents

New syntheses of 1-chloroalkylphosphinates

Morise, Xavier,Savignac, Philippe,Denis, Jean-Marc

, p. 2179 - 2185 (2007/10/03)

Different approaches to the synthesis of 1-chloroalkylphosphinates are described. Initially, we tried to extend a reaction described by Kabachnik for the preparation of chloromethylphosphinic acid chlorides [R1(Cl)P(O)CH2Cl] to C-substituted derivatives. We also considered the possibility of synthesizing the title compounds by routes already described for the formation of diethyl 1-chloroalkylphosphonates. Although these methods have allowed us to obtain several of the desired phosphinates, they suffer from limitations that restrict their synthetic applications. Finally, we have developed a more general approach that allows the formation of a wide range of phosphinates. It involves a selective P-C bond formation by reaction of MeMgCl and PhMgCl with phosphonochloridates, which are prepared by P-chlorination of 1-chloroalkylphosphonates.

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