Cas 1451368-65-2,ethyl 2-(cyclohex-1-en-1-yl)-2-diethoxyphosphoryloxyacetate

1451368-65-2

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Basic information

Product Name: ethyl 2-(cyclohex-1-en-1-yl)-2-diethoxyphosphoryloxyacetate
Synonyms: ethyl 2-(cyclohex-1-en-1-yl)-2-diethoxyphosphoryloxyacetate
CAS NO:1451368-65-2
Molecular Formula:
Molecular Weight: 320.323
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: ethyl 2-(cyclohex-1-en-1-yl)-2-diethoxyphosphoryloxyacetate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2-(cyclohex-1-en-1-yl)-2-diethoxyphosphoryloxyacetate(1451368-65-2)
EPA Substance Registry System: ethyl 2-(cyclohex-1-en-1-yl)-2-diethoxyphosphoryloxyacetate(1451368-65-2)

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: 1451368-65-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1451368-65-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,1,3,6 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1451368-65:
(9*1)+(8*4)+(7*5)+(6*1)+(5*3)+(4*6)+(3*8)+(2*6)+(1*5)=162
162 % 10 = 2
So 1451368-65-2 is a valid CAS Registry Number.

1451368-65-2Upstream product

138090-71-8 ethyl 2-diethylphosphono-2-(cyclohex-2-en-1-yloxy)acetate

1451368-65-2Downstream Products

1451368-65-2Relevant academic research and scientific papers

Bronsted base catalyzed [2,3]-Wittig/phospha-Brook tandem rearrangement sequence

Kondoh, Azusa,Terada, Masahiro

, p. 4568 - 4571 (2013/09/24)

A Bronsted base catalyzed rearrangement reaction of 2-allyloxy-2-phosphonoacetate derivatives was developed. This reaction proceeded via a [2,3]-Wittig rearrangement followed by a phospha-Brook rearrangement. This is the first example of a catalytic [2,3]-Wittig rearrangement initiated by a Bronsted base.

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