Cas 128669-64-7,2-Ethyl-3-((1R,5R)-5-isopropenyl-2-methyl-cyclohex-2-enylamino)-3H-quinazolin-4-one

128669-64-7

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Basic information

Product Name: 2-Ethyl-3-((1R,5R)-5-isopropenyl-2-methyl-cyclohex-2-enylamino)-3H-quinazolin-4-one
Synonyms:
CAS NO:128669-64-7
Molecular Formula:
Molecular Weight: 323.438
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: 2-Ethyl-3-((1R,5R)-5-isopropenyl-2-methyl-cyclohex-2-enylamino)-3H-quinazolin-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-Ethyl-3-((1R,5R)-5-isopropenyl-2-methyl-cyclohex-2-enylamino)-3H-quinazolin-4-one(128669-64-7)
EPA Substance Registry System: 2-Ethyl-3-((1R,5R)-5-isopropenyl-2-methyl-cyclohex-2-enylamino)-3H-quinazolin-4-one(128669-64-7)

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: 128669-64-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 128669-64-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,6,6 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 128669-64:
(8*1)+(7*2)+(6*8)+(5*6)+(4*6)+(3*9)+(2*6)+(1*4)=167
167 % 10 = 7
So 128669-64-7 is a valid CAS Registry Number.

128669-64-7Upstream product

128669-62-5 2-Ethyl-3-(2-hydroxy-4-isopropenyl-1-methyl-7-aza-bicyclo[4.1.0]hept-7-yl)-3H-quinazolin-4-one

128669-64-7Downstream Products

128669-64-7Relevant academic research and scientific papers

Regiospecific Radical-induced Cleavage of Aziridines: Syntheses of Allylic Amines and Pyrrolidines

Dickinson, Julia M.,Murphy, John A.

, p. 434 - 436 (1990)

The radical-induced cleavage of a series of fused aziridines has been found to proceed regiospecifically to produce C-N- bond cleavage, and the product radicals afford allylic amines or, in suitable cases, cyclise to form pyrrolidines.

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