Cas 1569453-40-2,N-(4-chloro-6,6,6-trifluorohexyl)-4-methylbenzenesulfonamide

1569453-40-2

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Basic information

Product Name: N-(4-chloro-6,6,6-trifluorohexyl)-4-methylbenzenesulfonamide
Synonyms: N-(4-chloro-6,6,6-trifluorohexyl)-4-methylbenzenesulfonamide
CAS NO:1569453-40-2
Molecular Formula:
Molecular Weight: 343.798
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: N-(4-chloro-6,6,6-trifluorohexyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(4-chloro-6,6,6-trifluorohexyl)-4-methylbenzenesulfonamide(1569453-40-2)
EPA Substance Registry System: N-(4-chloro-6,6,6-trifluorohexyl)-4-methylbenzenesulfonamide(1569453-40-2)

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: 1569453-40-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1569453-40-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,9,4,5 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1569453-40:
(9*1)+(8*5)+(7*6)+(6*9)+(5*4)+(4*5)+(3*3)+(2*4)+(1*0)=202
202 % 10 = 2
So 1569453-40-2 is a valid CAS Registry Number.

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1569453-40-2Relevant academic research and scientific papers

Chlorotrifluoromethylation method of alkene compounds using photoredox catalysis and CF3SO2Cl

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Paragraph 0063-0065; 0106-0107; 0311-0314, (2016/12/01)

The present invention relates to a chlorotrifluoromethylation method of an alkene compound using a photoredox catalyst and CF_3SO_2Cl. According to the present invention, the chlorotrifluoromethylation method of an alkene compound only generates SO_2 as a byproduct with one step of reaction and provides a source of -Cl and -CF_3 which are significant functional groups in pharmaceutical chemistry at the same time while having excellent regioselectivity of substituting -Cl to the carbon with a higher order.(AA) Time(BB) Conversion by ^1H NMR(%)COPYRIGHT KIPO 2016

Vicinal difunctionalization of alkenes: Chlorotrifluoromethylation with CF3SO2Cl by photoredox catalysis

Oh, Se Hwan,Malpani, Yashwardhan R.,Ha, Neul,Jung, Young-Sik,Han, Soo Bong

supporting information, p. 1310 - 1313 (2014/04/03)

Photoredox-catalyzed vicinal chlorotrifluoromethylation of alkene is described. In the presence of Ru(Phen)3Cl2, CF 3SO2Cl was used as a source for the CF3 radical and chloride ion under visible light irradiation. Various terminal and internal alkenes were transformed to their vicinal chlorotrifluoromethylated derivatives. Biologically active compounds were applied under the condition to obtain desired products, suggesting that the method could be feasible for late-stage modification in drug discovery.

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