Cas 89409-36-9,1-Biphenyl-4-yl-2,4-diphenyl-1,5,6,7-tetrahydro-quinoline-8-carbodithioic acid methyl ester

89409-36-9

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Basic information

Product Name: 1-Biphenyl-4-yl-2,4-diphenyl-1,5,6,7-tetrahydro-quinoline-8-carbodithioic acid methyl ester
Synonyms: 1-Biphenyl-4-yl-2,4-diphenyl-1,5,6,7-tetrahydro-quinoline-8-carbodithioic acid methyl ester
CAS NO:89409-36-9
Molecular Formula:
Molecular Weight: 527.754
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: 1-Biphenyl-4-yl-2,4-diphenyl-1,5,6,7-tetrahydro-quinoline-8-carbodithioic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1-Biphenyl-4-yl-2,4-diphenyl-1,5,6,7-tetrahydro-quinoline-8-carbodithioic acid methyl ester(89409-36-9)
EPA Substance Registry System: 1-Biphenyl-4-yl-2,4-diphenyl-1,5,6,7-tetrahydro-quinoline-8-carbodithioic acid methyl ester(89409-36-9)

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: 89409-36-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 89409-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,4,0 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89409-36:
(7*8)+(6*9)+(5*4)+(4*0)+(3*9)+(2*3)+(1*6)=169
169 % 10 = 9
So 89409-36-9 is a valid CAS Registry Number.

89409-36-9Upstream product

89409-31-4 1-Biphenyl-4-yl-8-methylsulfanylthiocarbonyl-2,4-diphenyl-5,6,7,8-tetrahydro-quinolinium; iodide

89409-36-9Downstream Products

89409-36-9Relevant academic research and scientific papers

Nucleophilic Displacements of N-Aryl and Heteroaryl Groups. Part 2. Pyrylium-mediated Transformations of Anilines into Aryl-sulphur Functionality

Katritzky, Alan R.,Langthorne, Ronald T.

, p. 2605 - 2609 (2007/10/02)

Carbon disulphide and methyl iodide converted the anhydrobases (3) into 8-pyridinium iodides (4) which afforded new pyridinium anhydrobases (5) with epoxide.These anhydrobases rearranged into the isomeric ketene S,S-dithioacetals (6), precursors for disulphides.

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