Cas 1201684-58-3,4,4-dimethyl-6-(4-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-quinoline

1201684-58-3

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Basic information

Product Name: 4,4-dimethyl-6-(4-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-quinoline
Synonyms: 4,4-dimethyl-6-(4-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-quinoline
CAS NO:1201684-58-3
Molecular Formula:
Molecular Weight: 305.343
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: 4,4-dimethyl-6-(4-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-quinoline(CAS DataBase Reference)
NIST Chemistry Reference: 4,4-dimethyl-6-(4-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-quinoline(1201684-58-3)
EPA Substance Registry System: 4,4-dimethyl-6-(4-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-quinoline(1201684-58-3)

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: 1201684-58-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1201684-58-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,6,8 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1201684-58:
(9*1)+(8*2)+(7*0)+(6*1)+(5*6)+(4*8)+(3*4)+(2*5)+(1*8)=123
123 % 10 = 3
So 1201684-58-3 is a valid CAS Registry Number.

1201684-58-3Upstream product

1201684-58-3Downstream Products

1201684-58-3Relevant academic research and scientific papers

ANNELATED N-HETEROCYCLIC SULFONAMIDES WITH OXADIAZOLONE HEADGROUP, PROCESSES FOR THEIR PREPARATION AND THEIR USE AS PHARMACEUTICALS

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Page/Page column 74-75, (2010/01/07)

Annelated N-heterocyclic sulfonamides with oxadiazolone headgroup, processes for their preparation and their use as pharmaceuticals The invention relates to annelated N-heterocyclic sulfonamides with oxadiazolone headgroup and to their physiologically acc

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