Cas 78394-79-3,2,5-Dimethyl-1-[2-oxo-2-(2,3,4-trimethyl-phenyl)-ethyl]-4-phenyl-pyridinium; bromide

78394-79-3

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Basic information

Product Name: 2,5-Dimethyl-1-[2-oxo-2-(2,3,4-trimethyl-phenyl)-ethyl]-4-phenyl-pyridinium; bromide
Synonyms:
CAS NO:78394-79-3
Molecular Formula:
Molecular Weight: 424.381
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: 2,5-Dimethyl-1-[2-oxo-2-(2,3,4-trimethyl-phenyl)-ethyl]-4-phenyl-pyridinium; bromide(CAS DataBase Reference)
NIST Chemistry Reference: 2,5-Dimethyl-1-[2-oxo-2-(2,3,4-trimethyl-phenyl)-ethyl]-4-phenyl-pyridinium; bromide(78394-79-3)
EPA Substance Registry System: 2,5-Dimethyl-1-[2-oxo-2-(2,3,4-trimethyl-phenyl)-ethyl]-4-phenyl-pyridinium; bromide(78394-79-3)

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: 78394-79-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 78394-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,3,9 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78394-79:
(7*7)+(6*8)+(5*3)+(4*9)+(3*4)+(2*7)+(1*9)=183
183 % 10 = 3
So 78394-79-3 is a valid CAS Registry Number.

78394-79-3Upstream product

78394-79-3Downstream Products

78394-85-1 6-Methyl-7-phenyl-2-(2,3,4-trimethyl-phenyl)-indolizine

78394-79-3Relevant academic research and scientific papers

SYNTHESIS OF 6-METHYL-2-ARYLINDOLIZINES CONTAINING PHENYL, p-ETHYLBENZYL, OR o,m,p-TRIMETHYLBENZYL SUBSTITUENTS AT C7

Prostakov, N.S.,Kuznetsov, V.I.,Romero, Ivan,Zvolinskii, V.P.

, p. 564 - 568 (2007/10/02)

In order to study the physiological activity of substituted indolizines 14 previously unknown indolizines, containing an aryl radical at C2 and a phenyl or substituted benzyl radical at C7, were obtained by the Chichibabin method fro

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