Cas 1173768-12-1,1-{3-[1-(4-methylphenyl)-3-phenylprop-2-ynyl]-1H-indol-2-yl}ethanone

1173768-12-1

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Basic information

Product Name: 1-{3-[1-(4-methylphenyl)-3-phenylprop-2-ynyl]-1H-indol-2-yl}ethanone
Synonyms: 1-{3-[1-(4-methylphenyl)-3-phenylprop-2-ynyl]-1H-indol-2-yl}ethanone
CAS NO:1173768-12-1
Molecular Formula:
Molecular Weight: 363.459
EINECS: N/A
Product Categories: N/A
Mol File: 1173768-12-1.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: 1-{3-[1-(4-methylphenyl)-3-phenylprop-2-ynyl]-1H-indol-2-yl}ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 1-{3-[1-(4-methylphenyl)-3-phenylprop-2-ynyl]-1H-indol-2-yl}ethanone(1173768-12-1)
EPA Substance Registry System: 1-{3-[1-(4-methylphenyl)-3-phenylprop-2-ynyl]-1H-indol-2-yl}ethanone(1173768-12-1)

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: 1173768-12-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1173768-12-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,7,6 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1173768-12:
(9*1)+(8*1)+(7*7)+(6*3)+(5*7)+(4*6)+(3*8)+(2*1)+(1*2)=171
171 % 10 = 1
So 1173768-12-1 is a valid CAS Registry Number.

1173768-12-1Upstream product

4264-35-1 2-acetylindole

1173768-12-1Downstream Products

1173768-37-0 3-benzyl-4-(4-methylphenyl)-1-(pyrrolidin-1-yl)-9H-carbazole

1173768-12-1Relevant articles and documents

Lewis Acid mediated aminobenzannulation reactions of δ-ketoalkynes: Synthesis of 1-aminocarbazoles and 9-aminopyrido[1,2-α]indoles

Facoetti, Diego,Abbiati, Giorgio,Rossi, Elisabetta

scheme or table, p. 2872 - 2882 (2009/08/09)

2-Acyl-N-propargylindoles 1 and 2-acyl-3-propargylindoles 5 undergo aminobenzannulation reactions with pyrrolidine in the presence of an appropriate Lewis acid to give 9-aminopyrido[1,2-α]indoles 6 and 1-aminocarbazoles 7, respectively. The selection of t

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