Cas 231289-66-0,2-amino-3-(2,5-dimethoxy-phenyl)-3-(2-dimethylamino-ethyl)-cyclohex-1-enecarbonitrile

231289-66-0

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Basic information

Product Name: 2-amino-3-(2,5-dimethoxy-phenyl)-3-(2-dimethylamino-ethyl)-cyclohex-1-enecarbonitrile
Synonyms:
CAS NO:231289-66-0
Molecular Formula:
Molecular Weight: 329.442
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-amino-3-(2,5-dimethoxy-phenyl)-3-(2-dimethylamino-ethyl)-cyclohex-1-enecarbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 2-amino-3-(2,5-dimethoxy-phenyl)-3-(2-dimethylamino-ethyl)-cyclohex-1-enecarbonitrile(231289-66-0)
EPA Substance Registry System: 2-amino-3-(2,5-dimethoxy-phenyl)-3-(2-dimethylamino-ethyl)-cyclohex-1-enecarbonitrile(231289-66-0)

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: 231289-66-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 231289-66-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,1,2,8 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 231289-66:
(8*2)+(7*3)+(6*1)+(5*2)+(4*8)+(3*9)+(2*6)+(1*6)=130
130 % 10 = 0
So 231289-66-0 is a valid CAS Registry Number.

231289-66-0Upstream product

18086-24-3 2-(2,5-dimethoxyphenyl)acetonitrile

231289-66-0Downstream Products

791571-94-3 2-(2,5-dimethoxy-phenyl)-2-(2-dimethylamino-ethyl)-cyclohexanone

231289-66-0Relevant academic research and scientific papers

An expedient synthesis of 9-keto-2-methyl-5-(dimethoxyphenyl)morphans

Linders, Joannes T. M.,Flippen-Anderson, Judith L.,George, Clifford F.,Rice, Kenner C.

, p. 3905 - 3908 (1999)

An expedient synthesis of ortho-methoxy substituted 9-keto-5- phenylmorphans has been developed, featuring a Thorpe-Zieger cyclization to construct the substituted 2-phenylcyclohexanone intermediate.

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