Cas 2512-40-5,1-[2-(3,4-dimethoxyphenyl)ethyl]-4a-methyl-1,3,4,4a,5,6-hexahydro-2H-cyclopenta[b]pyridin-2-one

2512-40-5

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Basic information

Product Name: 1-[2-(3,4-dimethoxyphenyl)ethyl]-4a-methyl-1,3,4,4a,5,6-hexahydro-2H-cyclopenta[b]pyridin-2-one
Synonyms:
CAS NO:2512-40-5
Molecular Formula:
Molecular Weight: 315.412
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-1,3,4,4a,5,6-hexahydro-2H-cyclopenta[b]pyridin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-[2-(3,4-dimethoxyphenyl)ethyl]-4a-methyl-1,3,4,4a,5,6-hexahydro-2H-cyclopenta[b]pyridin-2-one(2512-40-5)
EPA Substance Registry System: 1-[2-(3,4-dimethoxyphenyl)ethyl]-4a-methyl-1,3,4,4a,5,6-hexahydro-2H-cyclopenta[b]pyridin-2-one(2512-40-5)

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: 2512-40-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 2512-40-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,1 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2512-40:
(6*2)+(5*5)+(4*1)+(3*2)+(2*4)+(1*0)=55
55 % 10 = 5
So 2512-40-5 is a valid CAS Registry Number.

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2512-40-5Relevant 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 (2004)

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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