Cas 1176259-79-2,(1S,10bR)-(+)-1-(bis(phenylthio)methyl)-10b-butyl-8,9-dimethoxy-1,2,5,6-tetrahydropyrrolo[2,1-a]isoquinolin-3(10bH)-one

1176259-79-2

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Basic information

Product Name: (1S,10bR)-(+)-1-(bis(phenylthio)methyl)-10b-butyl-8,9-dimethoxy-1,2,5,6-tetrahydropyrrolo[2,1-a]isoquinolin-3(10bH)-one
Synonyms: (1S,10bR)-(+)-1-(bis(phenylthio)methyl)-10b-butyl-8,9-dimethoxy-1,2,5,6-tetrahydropyrrolo[2,1-a]isoquinolin-3(10bH)-one
CAS NO:1176259-79-2
Molecular Formula:
Molecular Weight: 533.756
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: (1S,10bR)-(+)-1-(bis(phenylthio)methyl)-10b-butyl-8,9-dimethoxy-1,2,5,6-tetrahydropyrrolo[2,1-a]isoquinolin-3(10bH)-one(CAS DataBase Reference)
NIST Chemistry Reference: (1S,10bR)-(+)-1-(bis(phenylthio)methyl)-10b-butyl-8,9-dimethoxy-1,2,5,6-tetrahydropyrrolo[2,1-a]isoquinolin-3(10bH)-one(1176259-79-2)
EPA Substance Registry System: (1S,10bR)-(+)-1-(bis(phenylthio)methyl)-10b-butyl-8,9-dimethoxy-1,2,5,6-tetrahydropyrrolo[2,1-a]isoquinolin-3(10bH)-one(1176259-79-2)

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: 1176259-79-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1176259-79-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,6,2,5 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1176259-79:
(9*1)+(8*1)+(7*7)+(6*6)+(5*2)+(4*5)+(3*9)+(2*7)+(1*9)=182
182 % 10 = 2
So 1176259-79-2 is a valid CAS Registry Number.

1176259-79-2Upstream product

3561-67-9 bis(phenylthio)methane

1176259-79-2Downstream Products

1176259-79-2Relevant academic research and scientific papers

Stereocontrolled conjugate additions to dihydroindolizinone systems. Synthesis of enantiopure polysubstituted tetrahydropyrrolo[2,1-a]isoquinolones

Camarero, Cristina,González-Temprano, Inés,Gómez-SanJuan, Asier,Arrasate, Sonia,Lete, Esther,Sotomayor, Nuria

, p. 5787 - 5798 (2009)

Conjugate addition reactions of various types of nucleophiles to the γ-lactam unit of dihydroindolizinone systems have been studied. The addition of cuprates, amines or stabilized carbanions requires the activation of the unsaturated bicyclic lactam with

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