Cas 110487-22-4,Dimethyl-{2-[3-(4-trifluoromethyl-phenyl)-quinolin-2-ylsulfanyl]-ethyl}-amine

110487-22-4

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Basic information

Product Name: Dimethyl-{2-[3-(4-trifluoromethyl-phenyl)-quinolin-2-ylsulfanyl]-ethyl}-amine
Synonyms:
CAS NO:110487-22-4
Molecular Formula:
Molecular Weight: 376.445
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: Dimethyl-{2-[3-(4-trifluoromethyl-phenyl)-quinolin-2-ylsulfanyl]-ethyl}-amine(CAS DataBase Reference)
NIST Chemistry Reference: Dimethyl-{2-[3-(4-trifluoromethyl-phenyl)-quinolin-2-ylsulfanyl]-ethyl}-amine(110487-22-4)
EPA Substance Registry System: Dimethyl-{2-[3-(4-trifluoromethyl-phenyl)-quinolin-2-ylsulfanyl]-ethyl}-amine(110487-22-4)

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: 110487-22-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 110487-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,4,8 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 110487-22:
(8*1)+(7*1)+(6*0)+(5*4)+(4*8)+(3*7)+(2*2)+(1*2)=94
94 % 10 = 4
So 110487-22-4 is a valid CAS Registry Number.

110487-22-4Upstream product

85274-99-3 N-phenyl-2-(4-(trifluoromethyl)phenyl)acetamide

110487-22-4Downstream Products

110487-22-4Relevant academic research and scientific papers

Synthesis and 5-Hydroxytryptamine Antagonist Activity of 2-thio>-3-phenylquinoline and Its Analogues

Blackburn, Thomas P.,Cox, Barry,Guildford, Allen J.,Count, David J. Le,Middlemiss, Derek N.,et al.

, p. 2252 - 2259 (2007/10/02)

A series of 2-quinolines substituted at the 3-position with alkyl, aryl, or heteroaryl groups has been prepared in the search for novel and selective 5-HT2 antagonists.The affinity of the compounds for 5-HT1 recep

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