Cas 1407181-98-9,(2S)-tert-butyl 2-((1R)-1-(2-(diethoxyphosphoryl)acetoxy)-2-oxocyclohex-3-en-1-yl)pyrrolidine-1-carboxylate

1407181-98-9

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Basic information

Product Name: (2S)-tert-butyl 2-((1R)-1-(2-(diethoxyphosphoryl)acetoxy)-2-oxocyclohex-3-en-1-yl)pyrrolidine-1-carboxylate
Synonyms: (2S)-tert-butyl 2-((1R)-1-(2-(diethoxyphosphoryl)acetoxy)-2-oxocyclohex-3-en-1-yl)pyrrolidine-1-carboxylate
CAS NO:1407181-98-9
Molecular Formula:
Molecular Weight: 459.477
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: (2S)-tert-butyl 2-((1R)-1-(2-(diethoxyphosphoryl)acetoxy)-2-oxocyclohex-3-en-1-yl)pyrrolidine-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (2S)-tert-butyl 2-((1R)-1-(2-(diethoxyphosphoryl)acetoxy)-2-oxocyclohex-3-en-1-yl)pyrrolidine-1-carboxylate(1407181-98-9)
EPA Substance Registry System: (2S)-tert-butyl 2-((1R)-1-(2-(diethoxyphosphoryl)acetoxy)-2-oxocyclohex-3-en-1-yl)pyrrolidine-1-carboxylate(1407181-98-9)

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: 1407181-98-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1407181-98-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,7,1,8 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1407181-98:
(9*1)+(8*4)+(7*0)+(6*7)+(5*1)+(4*8)+(3*1)+(2*9)+(1*8)=149
149 % 10 = 9
So 1407181-98-9 is a valid CAS Registry Number.

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1407181-98-9Relevant academic research and scientific papers

A facile approach to the synthesis of securinega alkaloids: stereoselective total synthesis of (-)-allonorsecurinine

Sathish Reddy, Alugubelli,Srihari, Pabbaraja

, p. 5926 - 5928,3 (2012)

A concise stereoselective total synthesis of alkaloid (-)-allonorsecurinine is described utilizing classical reactions such as Grignard, Aldol and Horner-Wittig reactions as the key steps.

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