Cas 1859-65-0,<i>N</i>-(1-methyl-2-phenyl-indol-3-yl)-acetamide

1859-65-0

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Basic information

Product Name: N-(1-methyl-2-phenyl-indol-3-yl)-acetamide
Synonyms:
CAS NO:1859-65-0
Molecular Formula:
Molecular Weight: 264.327
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: N-(1-methyl-2-phenyl-indol-3-yl)-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(1-methyl-2-phenyl-indol-3-yl)-acetamide(1859-65-0)
EPA Substance Registry System: N-(1-methyl-2-phenyl-indol-3-yl)-acetamide(1859-65-0)

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: 1859-65-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1859-65-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,5 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1859-65:
(6*1)+(5*8)+(4*5)+(3*9)+(2*6)+(1*5)=110
110 % 10 = 0
So 1859-65-0 is a valid CAS Registry Number.

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1859-65-0Relevant academic research and scientific papers

A versatile synthetic route to 11H-indolo[3,2-c]isoquinolines

Qu, Ji,Kumar, Naresh,Alamgir, Mahiuddin,Black, David StC.

scheme or table, p. 5628 - 5630 (2011/02/22)

A wide variety of indoloisoquinoline derivatives are prepared from the acid-catalyzed cyclization of 3-amido-2-phenylindoles, which in turn were obtained from the Beckmann rearrangement of 2-phenylindole-3-oximes.

An efficient base-mediated intramolecular condensation of 2-(disubstituted amino)-benzonitriles to 3-aminoindoles

Seong, Churl Min,Park, Chul Min,Choi, Jinil,Park, No Sang

scheme or table, p. 1029 - 1031 (2009/05/27)

A concise and versatile method for the preparation of 3-aminoindoles from 2-(disubstituted amino)-benzonitriles is described, and in situ functionalizations were illustrated.

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