Cas 1647159-58-7,1-(trifluoromethylthio)-(E)-(2-(4-methylbenzylidene))-1,2,3,4-tetrahydronaphthalene

1647159-58-7

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Basic information

Product Name: 1-(trifluoromethylthio)-(E)-(2-(4-methylbenzylidene))-1,2,3,4-tetrahydronaphthalene
Synonyms: 1-(trifluoromethylthio)-(E)-(2-(4-methylbenzylidene))-1,2,3,4-tetrahydronaphthalene
CAS NO:1647159-58-7
Molecular Formula:
Molecular Weight: 334.405
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-(trifluoromethylthio)-(E)-(2-(4-methylbenzylidene))-1,2,3,4-tetrahydronaphthalene(CAS DataBase Reference)
NIST Chemistry Reference: 1-(trifluoromethylthio)-(E)-(2-(4-methylbenzylidene))-1,2,3,4-tetrahydronaphthalene(1647159-58-7)
EPA Substance Registry System: 1-(trifluoromethylthio)-(E)-(2-(4-methylbenzylidene))-1,2,3,4-tetrahydronaphthalene(1647159-58-7)

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: 1647159-58-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1647159-58-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,4,7,1,5 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1647159-58:
(9*1)+(8*6)+(7*4)+(6*7)+(5*1)+(4*5)+(3*9)+(2*5)+(1*8)=197
197 % 10 = 7
So 1647159-58-7 is a valid CAS Registry Number.

1647159-58-7Upstream product

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1647159-58-7Relevant academic research and scientific papers

Direct trifluoromethylthiolation of alcohols under mild reaction conditions: Conversion of R-OH into R-SCF3

Nikolaienko, Pavlo,Pluta, Roman,Rueping, Magnus

supporting information, p. 9867 - 9870 (2014/08/18)

A direct process for the trifluoromethylthiolation of allylic and benzylic alcohols under mild conditions has been developed. A wide range of free alcohols underwent nucleophilic substitution in the presence of stable CuSCF3 and BF3·Et2O to give the corresponding products in good to excellent yields.

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