Cas 144039-63-4,1-[2-(3,4-Dimethoxy-phenyl)-ethyl]-6-oxo-2,3,3a,4,5,6-hexahydro-1H-indole-7-carboxylic acid tert-butyl ester

144039-63-4

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Basic information

Product Name: 1-[2-(3,4-Dimethoxy-phenyl)-ethyl]-6-oxo-2,3,3a,4,5,6-hexahydro-1H-indole-7-carboxylic acid tert-butyl ester
Synonyms: 1-[2-(3,4-Dimethoxy-phenyl)-ethyl]-6-oxo-2,3,3a,4,5,6-hexahydro-1H-indole-7-carboxylic acid tert-butyl ester
CAS NO:144039-63-4
Molecular Formula:
Molecular Weight: 401.503
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-Dimethoxy-phenyl)-ethyl]-6-oxo-2,3,3a,4,5,6-hexahydro-1H-indole-7-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1-[2-(3,4-Dimethoxy-phenyl)-ethyl]-6-oxo-2,3,3a,4,5,6-hexahydro-1H-indole-7-carboxylic acid tert-butyl ester(144039-63-4)
EPA Substance Registry System: 1-[2-(3,4-Dimethoxy-phenyl)-ethyl]-6-oxo-2,3,3a,4,5,6-hexahydro-1H-indole-7-carboxylic acid tert-butyl ester(144039-63-4)

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: 144039-63-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 144039-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,0,3 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 144039-63:
(8*1)+(7*4)+(6*4)+(5*0)+(4*3)+(3*9)+(2*6)+(1*3)=114
114 % 10 = 4
So 144039-63-4 is a valid CAS Registry Number.

144039-63-4Upstream product

144039-63-4Downstream Products

64705-40-4 1-(3,4-dimethoxy-phenethyl)-1,2,3,3a,4,5-hexahydro-indol-6-one

144039-63-4Relevant academic research and scientific papers

Synthesis of hexahydroindol-6-ones by reaction of 2-methylthiopyrrolinium salts with Nazarov reagents

Michael,Zwane

, p. 4755 - 4758 (2007/10/02)

The title compounds 6-8 were prepared by variations of a route commencing with base-promoted condensation of N-substituted 2-methylthio-Δ1-pyrrolinium iodides 2 with Nazarov and related reagents, followed by further manipulation of substituted enamines 11-14.

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