Cas 109322-72-7,[(Z)-2-(4-Methoxy-phenyl)-1-(2-trimethylsilanyl-ethoxy)-vinyl]-phosphonic acid diethyl ester

109322-72-7

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Basic information

Product Name: [(Z)-2-(4-Methoxy-phenyl)-1-(2-trimethylsilanyl-ethoxy)-vinyl]-phosphonic acid diethyl ester
Synonyms:
CAS NO:109322-72-7
Molecular Formula:
Molecular Weight: 386.5
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: [(Z)-2-(4-Methoxy-phenyl)-1-(2-trimethylsilanyl-ethoxy)-vinyl]-phosphonic acid diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(Z)-2-(4-Methoxy-phenyl)-1-(2-trimethylsilanyl-ethoxy)-vinyl]-phosphonic acid diethyl ester(109322-72-7)
EPA Substance Registry System: [(Z)-2-(4-Methoxy-phenyl)-1-(2-trimethylsilanyl-ethoxy)-vinyl]-phosphonic acid diethyl ester(109322-72-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 109322-72-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 109322-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,3,2 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 109322-72:
(8*1)+(7*0)+(6*9)+(5*3)+(4*2)+(3*2)+(2*7)+(1*2)=107
107 % 10 = 7
So 109322-72-7 is a valid CAS Registry Number.

109322-72-7Upstream product

109322-72-7Downstream Products

109322-80-7 2-Trimethylsilylethyl 4-methoxymandelate

109322-72-7Relevant academic research and scientific papers

A NEW PROCEDURE FOR HOMOLOGATION OF CARBONYL COMPOUNDS TO α-HYDROXY-CARBOXYLIC ESTERS BY MEANS OF DIETHYL-PHOSPHONATE

Binder, Josef,Zbiral, Erich

, p. 5829 - 5832 (1986)

A synthesis of α-hydroxyesters 5 using the Peterson olefination of the α-trimethylsilyl-substituted phosphonate 2 to vinylphosphonates 3 followed by hydroxylation with catalytical amounts of OsO4 has been developed.

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