Cas 741266-34-2,11,12-dimethoxy-1,2,4a,5-tetrahydro-4<i>H</i>-indolo[7a,1-<i>a</i>]isoquinoline-3,6-dione

741266-34-2

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Basic information

Product Name: 11,12-dimethoxy-1,2,4a,5-tetrahydro-4H-indolo[7a,1-a]isoquinoline-3,6-dione
Synonyms: 11,12-dimethoxy-1,2,4a,5-tetrahydro-4H-indolo[7a,1-a]isoquinoline-3,6-dione
CAS NO:741266-34-2
Molecular Formula:
Molecular Weight: 313.353
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: 11,12-dimethoxy-1,2,4a,5-tetrahydro-4H-indolo[7a,1-a]isoquinoline-3,6-dione(CAS DataBase Reference)
NIST Chemistry Reference: 11,12-dimethoxy-1,2,4a,5-tetrahydro-4H-indolo[7a,1-a]isoquinoline-3,6-dione(741266-34-2)
EPA Substance Registry System: 11,12-dimethoxy-1,2,4a,5-tetrahydro-4H-indolo[7a,1-a]isoquinoline-3,6-dione(741266-34-2)

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: 741266-34-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 741266-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,1,2,6 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 741266-34:
(8*7)+(7*4)+(6*1)+(5*2)+(4*6)+(3*6)+(2*3)+(1*4)=152
152 % 10 = 2
So 741266-34-2 is a valid CAS Registry Number.

741266-34-2Upstream product

32161-30-1 (S)-3,4-dimethoxyphenylalanine

741266-34-2Downstream Products

741266-34-2Relevant academic research and scientific papers

A formal asymmetric synthesis of both enantiomers of the Erythrina alkaloid 3-demethoxyerythratidinone

Allin, Steven M.,Streetley, Guy B.,Slater, Martin,James, Stella L.,Martin, William P.

, p. 5493 - 5496 (2007/10/05)

A formal asymmetric synthesis of both enantiomers of the Erythrina alkaloid 3-demethoxyerythratidinone is reported through the application of a highly functionalised lactam template as an N-acyliminium precursor.

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