Cas 1108633-56-2,2-mercapto-1,2,2-triphenylethyl 2-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]phenyl sulfide

1108633-56-2

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Basic information

Product Name: 2-mercapto-1,2,2-triphenylethyl 2-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]phenyl sulfide
Synonyms: 2-mercapto-1,2,2-triphenylethyl 2-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]phenyl sulfide
CAS NO:1108633-56-2
Molecular Formula:
Molecular Weight: 564.615
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-mercapto-1,2,2-triphenylethyl 2-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]phenyl sulfide(CAS DataBase Reference)
NIST Chemistry Reference: 2-mercapto-1,2,2-triphenylethyl 2-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]phenyl sulfide(1108633-56-2)
EPA Substance Registry System: 2-mercapto-1,2,2-triphenylethyl 2-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]phenyl sulfide(1108633-56-2)

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: 1108633-56-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1108633-56-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,8,6,3 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1108633-56:
(9*1)+(8*1)+(7*0)+(6*8)+(5*6)+(4*3)+(3*3)+(2*5)+(1*6)=132
132 % 10 = 2
So 1108633-56-2 is a valid CAS Registry Number.

1108633-56-2Upstream product

1108633-52-8 2-acetylthio-1,2,2-triphenylethyl 2-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]phenyl sulfide

1108633-56-2Downstream Products

1108633-56-2Relevant academic research and scientific papers

Structure and properties of a sulfur(IV)-sulfur(II)-bond compound: Reversible conversion of a sulfur-substituted organosulfurane into a thiol

Kano, Naokazu,Itoh, Yusuke,Watanabe, Yuki,Kusaka, Shinpei,Kawashima, Takayuki

, p. 9430 - 9433 (2008)

(Figure Presented) A highly polar hypervalent SIV - S II bond was formed in the synthesis of a sulfur-substituted sulfurane (see scheme), which was crystallographically characterized. Reduction of the 1,2-dithietane gives the corresp

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