Cas 2118-97-0,1-[2-(3,4-dimethoxyphenyl)ethyl]-4a-methyl-3,4,4a,5,6,7-hexahydro-1H-quinolin-2-one

2118-97-0

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Basic information

Product Name: 1-[2-(3,4-dimethoxyphenyl)ethyl]-4a-methyl-3,4,4a,5,6,7-hexahydro-1H-quinolin-2-one
Synonyms: 1-[2-(3,4-dimethoxyphenyl)ethyl]-4a-methyl-3,4,4a,5,6,7-hexahydro-1H-quinolin-2-one
CAS NO:2118-97-0
Molecular Formula:
Molecular Weight: 329.439
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: 1-[2-(3,4-dimethoxyphenyl)ethyl]-4a-methyl-3,4,4a,5,6,7-hexahydro-1H-quinolin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-[2-(3,4-dimethoxyphenyl)ethyl]-4a-methyl-3,4,4a,5,6,7-hexahydro-1H-quinolin-2-one(2118-97-0)
EPA Substance Registry System: 1-[2-(3,4-dimethoxyphenyl)ethyl]-4a-methyl-3,4,4a,5,6,7-hexahydro-1H-quinolin-2-one(2118-97-0)

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: 2118-97-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 2118-97-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,1 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2118-97:
(6*2)+(5*1)+(4*1)+(3*8)+(2*9)+(1*7)=70
70 % 10 = 0
So 2118-97-0 is a valid CAS Registry Number.

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2118-97-0Relevant academic research and scientific papers

Electrophilic-induced cyclization reaction of hexahydroindolinone derivatives and its application toward the synthesis of (±)- erysotramidine

Padwa, Albert,Lee, Hyoung Ik,Rashatasakhon, Paitoon,Rose, Mickea

, p. 8209 - 8218 (2007/10/03)

A convenient synthesis of variously substituted octahydroindolo[7a,1a]- isoquinolinones has been achieved by an acid-induced cyclization of hexahydroindolinones bearing tethered phenethyl groups. The formation of a single lactam diastereomer is the result

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