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

481679-70-3

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481679-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 481679-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,1,6,7 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 481679-70:
(8*4)+(7*8)+(6*1)+(5*6)+(4*7)+(3*9)+(2*7)+(1*0)=193
193 % 10 = 3
So 481679-70-3 is a valid CAS Registry Number.

481679-70-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(dimethoxyphosphorylmethyl)-4-methylsulfanylbenzene

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:481679-70-3 SDS

481679-70-3Relevant academic research and scientific papers

Deposition of ordered layers of tetralactam macrocycles and ether rotaxanes on pyridine-terminated self-assembled monolayers on gold

Richter, Sebastian,Poppenberg, Johannes,Traulsen, Christoph H.-H.,Sokolowski, Anja,Sattler, Dominik,Schalley, Christoph A.,Darlatt, Erik,Unger, Wolfgang E. S.

supporting information, p. 16289 - 16297,9 (2020/09/09)

The deposition of tetralactam macrocycles and the corresponding benzyl ether rotaxanes on gold substrates is investigated for the first time exploiting metallo-supramolecular chemistry. Two pyridine-terminated self-assembled monolayers (SAMs) are develope

Alkyl-bridged substituted 8-arylquinolines as highly potent PDE IV inhibitors

Lacombe, Patrick,Chauret, Nathalie,Claveau, David,Day, Stephen,Deschenes, Denis,Dube, Daniel,Gallant, Michel,Girard, Yves,Huang, Zheng,Laliberte, France,Levesque, Jean-Francois,Liu, Susana,Macdonald, Dwight,Mancini, Joseph A.,Masson, Paul,Nicholson, Donald W.,Nicoll-Griffith, Deborah A.,Salem, Myriam,Styhler, Angela,Young, Robert N.

scheme or table, p. 5266 - 5269 (2010/03/31)

Substituted 8-arylquinoline analogs bearing alkyl-linked side chain were identified as potent inhibitors of type 4 phophodiesterase. These compounds address the potential liabilities of the clinical candidate L-454560. The pharmacokinetic profile of the b

Efficient and rapid synthesis of oligo(p-phenylenevinylene) via iterative coherent approach

Xue, Cuihua,Luo, Fen-Tair

, p. 4417 - 4421 (2007/10/03)

A general and controlled bidirectional growth strategy enables a very rapid and efficient construction of OPV compounds possessing functional groups such as aldehyde and mercapto groups at both ends. The strategy employs only one reaction type with high y

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