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73750-69-3

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73750-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73750-69-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,5 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73750-69:
(7*7)+(6*3)+(5*7)+(4*5)+(3*0)+(2*6)+(1*9)=143
143 % 10 = 3
So 73750-69-3 is a valid CAS Registry Number.

73750-69-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,methoxy(methyl)phosphinate

1.2 Other means of identification

Product number -
Other names Methyl-phosphonsaeure-monomethylester,Natrium-Salz

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:73750-69-3 SDS

73750-69-3Relevant articles and documents

THE REACTION OF ALKANEPHOSPHONIC ACID ESTERS WITH METALS

Koch, P.,Rumpel, H.,Sutter, P.,Weis, C. D.

, p. 75 - 86 (2007/10/02)

The reaction of dialkyl alkanephosphosnates (methyl, ethyl, isopropyl) with alkali and earth alkali metals, respectively, has been investigated.These metals reacted with phosphonates yielding the corresponding salts of monoalkyl alkanephosphonates with the evolution of a mixture of low molecular weight gaseous products the composition of which was quantitatively determined by gas chromatographic methods.The gaseous products could be traced to the primary formation of radical fragments originating from cleavage of either the carbon-oxygen or the phosphorus-oxygen bonds.Lower alkanes were formed predominantly, but there were also traces of acetylene and also of benzene.Diisopropyl methylphosphonate showed to a large extent cleavage of the carbon-phosphorus bond, yielding a mixture of the salts of isopropylphosphonite and isopropyl methylphosphonate.Reaction mechanisms were advanced to explain some of the results.Key words: Dialkyl alkanephosphonates; metal salts of alkyl alkanephosphonates; GC of gas mixtures; P-C bond cleavage; P-O bond cleavage; reaction mechanism.

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