Cas 797791-51-6,(1-allyl-2-methoxy-cyclohexa-2,5-dienyl)-pyrrolidin-1-yl-methanone

797791-51-6

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Basic information

Product Name: (1-allyl-2-methoxy-cyclohexa-2,5-dienyl)-pyrrolidin-1-yl-methanone
Synonyms: (1-allyl-2-methoxy-cyclohexa-2,5-dienyl)-pyrrolidin-1-yl-methanone
CAS NO:797791-51-6
Molecular Formula:
Molecular Weight: 247.337
EINECS: N/A
Product Categories: N/A
Mol File: 797791-51-6.mol
Article Data: 1

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: (1-allyl-2-methoxy-cyclohexa-2,5-dienyl)-pyrrolidin-1-yl-methanone(CAS DataBase Reference)
NIST Chemistry Reference: (1-allyl-2-methoxy-cyclohexa-2,5-dienyl)-pyrrolidin-1-yl-methanone(797791-51-6)
EPA Substance Registry System: (1-allyl-2-methoxy-cyclohexa-2,5-dienyl)-pyrrolidin-1-yl-methanone(797791-51-6)

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: 797791-51-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 797791-51-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,7,7,9 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 797791-51:
(8*7)+(7*9)+(6*7)+(5*7)+(4*9)+(3*1)+(2*5)+(1*1)=246
246 % 10 = 6
So 797791-51-6 is a valid CAS Registry Number.

797791-51-6Upstream product

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797791-51-6Relevant articles and documents

Sequential Birch reduction-allylation and Cope rearrangement of o-anisic acid derivatives

Malachowski, William P.,Banerji, Marisha

, p. 8183 - 8185 (2004)

A new method for the construction of quaternary centers on cycloalkane rings is reported. The Cope rearrangement of 4-methyl-2-allyl-2-(N-pyrrolidinyl) -carboxamide-3-cyclohexenone yields 4-methyl-4-allyl-2-(N-pyrrolidinyl)- carboxamide-2-cyclohexenone in high yield. The rearrangement substrates are easily generated from Birch reduction-allylation of o-anisic acid derivatives.

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