Cas 1413432-55-9,(6aR,7R,10aS)-1-(4-chlorophenyl)-2-iodo-7,9-dimethyl-6a,7-dihydropyrrolo[2,1-i]indole-3,6,8(5H)-trione

1413432-55-9

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Basic information

Product Name: (6aR,7R,10aS)-1-(4-chlorophenyl)-2-iodo-7,9-dimethyl-6a,7-dihydropyrrolo[2,1-i]indole-3,6,8(5H)-trione
Synonyms: (6aR,7R,10aS)-1-(4-chlorophenyl)-2-iodo-7,9-dimethyl-6a,7-dihydropyrrolo[2,1-i]indole-3,6,8(5H)-trione
CAS NO:1413432-55-9
Molecular Formula:
Molecular Weight: 467.69
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: (6aR,7R,10aS)-1-(4-chlorophenyl)-2-iodo-7,9-dimethyl-6a,7-dihydropyrrolo[2,1-i]indole-3,6,8(5H)-trione(CAS DataBase Reference)
NIST Chemistry Reference: (6aR,7R,10aS)-1-(4-chlorophenyl)-2-iodo-7,9-dimethyl-6a,7-dihydropyrrolo[2,1-i]indole-3,6,8(5H)-trione(1413432-55-9)
EPA Substance Registry System: (6aR,7R,10aS)-1-(4-chlorophenyl)-2-iodo-7,9-dimethyl-6a,7-dihydropyrrolo[2,1-i]indole-3,6,8(5H)-trione(1413432-55-9)

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: 1413432-55-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1413432-55-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,3,4,3 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1413432-55:
(9*1)+(8*4)+(7*1)+(6*3)+(5*4)+(4*3)+(3*2)+(2*5)+(1*5)=119
119 % 10 = 9
So 1413432-55-9 is a valid CAS Registry Number.

1413432-55-9Upstream product

1413432-43-5 2-(4-(4-chlorophenyl)-3-iodo-7,9-dimethyl-2,8-dioxo-1-azaspiro[4.5]deca-3,6,9-trien-1-yl)acetaldehyde

1413432-55-9Downstream Products

1413432-55-9Relevant academic research and scientific papers

Diastereoselective and enantioselective desymmetrization of α-substituted cyclohexadienones via intramolecular stetter reaction

Jia, Min-Qiang,Liu, Chuan,You, Shu-Li

, p. 10996 - 11001 (2012)

Highly diastereoselective and enantioselective desymmetrization of α-substituted cyclohexadienones via NHC-catalyzed intramolecular Stetter reaction was realized. Amino-indanol derived triazolium salt bearing a C 6F5 group was found to be the optimal catalyst precursor in the intramolecular Stetter reaction furnishing tricyclic products bearing multi-stereocenters in up to 96% yield and >99% ee.

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