Cas 1234701-84-8,2-(3-ethylsulfanyl-4,4,4-trifluoro-1-hydroxy-2-phenylbut-2-enyl)-cyclohex-2-en-1-one

1234701-84-8

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Basic information

Product Name: 2-(3-ethylsulfanyl-4,4,4-trifluoro-1-hydroxy-2-phenylbut-2-enyl)-cyclohex-2-en-1-one
Synonyms: 2-(3-ethylsulfanyl-4,4,4-trifluoro-1-hydroxy-2-phenylbut-2-enyl)-cyclohex-2-en-1-one
CAS NO:1234701-84-8
Molecular Formula:
Molecular Weight: 356.409
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-(3-ethylsulfanyl-4,4,4-trifluoro-1-hydroxy-2-phenylbut-2-enyl)-cyclohex-2-en-1-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3-ethylsulfanyl-4,4,4-trifluoro-1-hydroxy-2-phenylbut-2-enyl)-cyclohex-2-en-1-one(1234701-84-8)
EPA Substance Registry System: 2-(3-ethylsulfanyl-4,4,4-trifluoro-1-hydroxy-2-phenylbut-2-enyl)-cyclohex-2-en-1-one(1234701-84-8)

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: 1234701-84-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1234701-84-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,4,7,0 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1234701-84:
(9*1)+(8*2)+(7*3)+(6*4)+(5*7)+(4*0)+(3*1)+(2*8)+(1*4)=128
128 % 10 = 8
So 1234701-84-8 is a valid CAS Registry Number.

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1234701-84-8Relevant academic research and scientific papers

Application of Sonogashira and Baylis-Hillman reactions with β-trifluoromethylated acroleins

Zouaoui, Emna,Gaied, Mohamed Moncef El

experimental part, p. 5 - 7 (2010/05/19)

The reaction of alkynes with 2-phenyl-3-iodo-4,4,4-trifluorobut-2-enal in the presence of palladium (0) is reported (Sonogashira reaction). Moreover, 2-(hydroxytrifluoromethylalkenyl)cyclohexenones have been prepared by the reaction of cyclohexenone and β

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