Cas 451502-83-3,{(E)-3-[3-(4-Methoxy-phenyl)-2-oxo-oxazolidin-4-yl]-allyl}-phosphonic acid diethyl ester

451502-83-3

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Basic information

Product Name: {(E)-3-[3-(4-Methoxy-phenyl)-2-oxo-oxazolidin-4-yl]-allyl}-phosphonic acid diethyl ester
Synonyms: {(E)-3-[3-(4-Methoxy-phenyl)-2-oxo-oxazolidin-4-yl]-allyl}-phosphonic acid diethyl ester
CAS NO:451502-83-3
Molecular Formula:
Molecular Weight: 369.354
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: {(E)-3-[3-(4-Methoxy-phenyl)-2-oxo-oxazolidin-4-yl]-allyl}-phosphonic acid diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {(E)-3-[3-(4-Methoxy-phenyl)-2-oxo-oxazolidin-4-yl]-allyl}-phosphonic acid diethyl ester(451502-83-3)
EPA Substance Registry System: {(E)-3-[3-(4-Methoxy-phenyl)-2-oxo-oxazolidin-4-yl]-allyl}-phosphonic acid diethyl ester(451502-83-3)

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: 451502-83-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 451502-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,1,5,0 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 451502-83:
(8*4)+(7*5)+(6*1)+(5*5)+(4*0)+(3*2)+(2*8)+(1*3)=123
123 % 10 = 3
So 451502-83-3 is a valid CAS Registry Number.

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451502-83-3Relevant academic research and scientific papers

In situ enzymatic screening (ISES): A tool for catalyst discovery and reaction development

Berkowitz, David B.,Bose, Mohua,Choi, Sungjo

, p. 1603 - 1607 (2007/10/03)

Can enzymes help organic chemists identify new transition-metal catalysts? The first example of the in situ enzymatic monitoring of an organic transformation is described. Thus, a transition-metal-mediated allylic-amination reaction in the organic layer (

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