Cas 79139-01-8,Methyl-[(4S,5S)-5-(2-methyl-propenyl)-1,2,2a,3,4,5-hexahydro-benzo[cd]indol-4-yl]-amine

79139-01-8

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Basic information

Product Name: Methyl-[(4S,5S)-5-(2-methyl-propenyl)-1,2,2a,3,4,5-hexahydro-benzo[cd]indol-4-yl]-amine
Synonyms:
CAS NO:79139-01-8
Molecular Formula:
Molecular Weight: 242.364
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: Methyl-[(4S,5S)-5-(2-methyl-propenyl)-1,2,2a,3,4,5-hexahydro-benzo[cd]indol-4-yl]-amine(CAS DataBase Reference)
NIST Chemistry Reference: Methyl-[(4S,5S)-5-(2-methyl-propenyl)-1,2,2a,3,4,5-hexahydro-benzo[cd]indol-4-yl]-amine(79139-01-8)
EPA Substance Registry System: Methyl-[(4S,5S)-5-(2-methyl-propenyl)-1,2,2a,3,4,5-hexahydro-benzo[cd]indol-4-yl]-amine(79139-01-8)

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: 79139-01-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 79139-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,3 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79139-01:
(7*7)+(6*9)+(5*1)+(4*3)+(3*9)+(2*0)+(1*1)=148
148 % 10 = 8
So 79139-01-8 is a valid CAS Registry Number.

79139-01-8Upstream product

79133-75-8 (4S,5S)-4-(Methanesulfonyl-methyl-amino)-5-(2-methyl-propenyl)-4,5-dihydro-3H-benzo[cd]indole-1-carboxylic acid methyl ester

79139-01-8Downstream Products

79139-01-8Relevant academic research and scientific papers

TOTAL SYNTHESIS OF ERGOT ALKALOID, (+/-)-6,7-SECOAGROCLAVINE

Somei, Masanori,Yamada, Fumio,Karasawa, Yoshio,Kaneko, Chikara

, p. 615 - 618 (1981)

Ergot alkaloid, (+/-)-6,7-secoagroclavine was synthesized form 2-methyl-5-nitroisoquinolinium iodide by three routes.In the course of the study, a novel intra-molecular γ-alkylation of allyl alcohol was found.Reaction of Grignard reagents with nitroalkanes to afford N-alkyl hydroxylamines was effectively used in the present synthesis.

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