Cas 783334-61-2,[1R-(1β,2α,3β,4β)]-6-methoxy2,3,4-tri(methoxymethyl)-1,2,3,4-tetrahydro-1-(phenylthio)-2H-[1,3]benzodioxolo[5,6-c]-[1]benzopyran-6-one

783334-61-2

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Basic information

Product Name: [1R-(1β,2α,3β,4β)]-6-methoxy2,3,4-tri(methoxymethyl)-1,2,3,4-tetrahydro-1-(phenylthio)-2H-[1,3]benzodioxolo[5,6-c]-[1]benzopyran-6-one
Synonyms: [1R-(1β,2α,3β,4β)]-6-methoxy2,3,4-tri(methoxymethyl)-1,2,3,4-tetrahydro-1-(phenylthio)-2H-[1,3]benzodioxolo[5,6-c]-[1]benzopyran-6-one
CAS NO:783334-61-2
Molecular Formula:
Molecular Weight: 562.595
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: [1R-(1β,2α,3β,4β)]-6-methoxy2,3,4-tri(methoxymethyl)-1,2,3,4-tetrahydro-1-(phenylthio)-2H-[1,3]benzodioxolo[5,6-c]-[1]benzopyran-6-one(CAS DataBase Reference)
NIST Chemistry Reference: [1R-(1β,2α,3β,4β)]-6-methoxy2,3,4-tri(methoxymethyl)-1,2,3,4-tetrahydro-1-(phenylthio)-2H-[1,3]benzodioxolo[5,6-c]-[1]benzopyran-6-one(783334-61-2)
EPA Substance Registry System: [1R-(1β,2α,3β,4β)]-6-methoxy2,3,4-tri(methoxymethyl)-1,2,3,4-tetrahydro-1-(phenylthio)-2H-[1,3]benzodioxolo[5,6-c]-[1]benzopyran-6-one(783334-61-2)

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: 783334-61-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 783334-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,3,3,3 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 783334-61:
(8*7)+(7*8)+(6*3)+(5*3)+(4*3)+(3*4)+(2*6)+(1*1)=182
182 % 10 = 2
So 783334-61-2 is a valid CAS Registry Number.

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783334-61-2Relevant academic research and scientific papers

A short route to enantiomerically pure benzophenanthridinone skeletons synthesis of lactone analogues of narciclasine and lycoricidine

Ibn-Ahmed, Said,Khaldi, Mustapha,Chretien, Francoise,Chapleur, Yves

, p. 6722 - 6731 (2007/10/03)

Condensation of functionalized o-toluamide anions on a carbohydrate-derived lactone, followed by intramolecular aldol cyclization, provides enantiomerically pure 2-arylcyclohexenones. Different approaches for the stereoselective transformation of the carb

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