Cas 1169948-92-8,(3S,4R)-9-benzyl-4-propyl-2,3,4,9-tetrahydro-1H-carbazole-3-carbaldehyde

1169948-92-8

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Basic information

Product Name: (3S,4R)-9-benzyl-4-propyl-2,3,4,9-tetrahydro-1H-carbazole-3-carbaldehyde
Synonyms: (3S,4R)-9-benzyl-4-propyl-2,3,4,9-tetrahydro-1H-carbazole-3-carbaldehyde
CAS NO:1169948-92-8
Molecular Formula:
Molecular Weight: 331.458
EINECS: N/A
Product Categories: N/A
Mol File: 1169948-92-8.mol
Article Data: 1

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: (3S,4R)-9-benzyl-4-propyl-2,3,4,9-tetrahydro-1H-carbazole-3-carbaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4R)-9-benzyl-4-propyl-2,3,4,9-tetrahydro-1H-carbazole-3-carbaldehyde(1169948-92-8)
EPA Substance Registry System: (3S,4R)-9-benzyl-4-propyl-2,3,4,9-tetrahydro-1H-carbazole-3-carbaldehyde(1169948-92-8)

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: 1169948-92-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1169948-92-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,9,9,4 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1169948-92:
(9*1)+(8*1)+(7*6)+(6*9)+(5*9)+(4*4)+(3*8)+(2*9)+(1*2)=218
218 % 10 = 8
So 1169948-92-8 is a valid CAS Registry Number.

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1169948-92-8Relevant articles and documents

Organocatalytic multiple cascade reactions: A new strategy for the construction of enantioenriched tetrahydrocarbazoles

Cao, Yi-Ju,Cheng, Hong-Gang,Lu, Liang-Qiu,Zhang, Ji-Ji,Cheng, Ying,Chen, Jia-Rong,Xiao, Wen-Jing

, p. 617 - 623 (2011/04/23)

A novel cascade Friedel-Crafts alkylation/Michael addition/aromatization reaction of 2-vinylindoles with α,β-unsaturated aldehydes has been developed for the construction of functionalized tetrahydrocarbazoles. The products were obtained in up to 97% yiel

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