Cas 810681-59-5,6H-Pyrido[2,1-i]indol-6-one,3,4,7,7a,8,9,10,11-octahydro-2,7a-dimethyl-(9CI)

810681-59-5

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Basic information

Product Name: 6H-Pyrido[2,1-i]indol-6-one,3,4,7,7a,8,9,10,11-octahydro-2,7a-dimethyl-(9CI)
Synonyms: 6H-Pyrido[2,1-i]indol-6-one,3,4,7,7a,8,9,10,11-octahydro-2,7a-dimethyl-(9CI)
CAS NO:810681-59-5
Molecular Formula: C14H21NO
Molecular Weight: 219.32264
EINECS: N/A
Product Categories: METHYL
Mol File: 810681-59-5.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 6H-Pyrido[2,1-i]indol-6-one,3,4,7,7a,8,9,10,11-octahydro-2,7a-dimethyl-(9CI)(CAS DataBase Reference)
NIST Chemistry Reference: 6H-Pyrido[2,1-i]indol-6-one,3,4,7,7a,8,9,10,11-octahydro-2,7a-dimethyl-(9CI)(810681-59-5)
EPA Substance Registry System: 6H-Pyrido[2,1-i]indol-6-one,3,4,7,7a,8,9,10,11-octahydro-2,7a-dimethyl-(9CI)(810681-59-5)

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: 810681-59-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 810681-59-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,0,6,8 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 810681-59:
(8*8)+(7*1)+(6*0)+(5*6)+(4*8)+(3*1)+(2*5)+(1*9)=155
155 % 10 = 5
So 810681-59-5 is a valid CAS Registry Number.

810681-59-5Upstream product

810681-59-5Downstream Products

810681-59-5Relevant 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 (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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