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Phosphonic acid, methyl-, bis(4-(methylthio)phenyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88847-60-3

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88847-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88847-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,8,4 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88847-60:
(7*8)+(6*8)+(5*8)+(4*4)+(3*7)+(2*6)+(1*0)=193
193 % 10 = 3
So 88847-60-3 is a valid CAS Registry Number.

88847-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[methyl-(4-methylsulfanylphenoxy)phosphoryl]oxy-4-methylsulfanylbenzene

1.2 Other means of identification

Product number -
Other names bis(4-methylthiophenyl) methylphosphonate

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:88847-60-3 SDS

88847-60-3Relevant academic research and scientific papers

PHOTOLYSIS OF ARYL ESTERS OF TRI- AND TETRACOORDINATED PHOSPHORUS COMPOUNDS

Shi, Min,Yamamoto, Kiichi,Okamoto, Yoshiki,Takamuku, Setsuo

, p. 1 - 14 (2007/10/02)

Upon UV excitation in methanol, some diaryl esters of alkly- or alkenyl phosphonates underwent an elimination of two aryl groups to give biaryls and the corresponding alkyl- or alkenylphosphonic acids.Tris(4-methoxyphenyl) phosphite also underwent a similar elimination to give 4,4'-dimethoxybiphenyl and 4-methoxyphenyl phosphonate.This interesting biaryl elimination was confirmed to proceed via a singlet intramolecular excimer by means of fluorescence spectra and Stern-Volmer analysis.

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