Cas 105479-67-2,Benzene, 1,1'-[(3,3,4,4-tetramethyl-1,5-hexadiene-1,6-diyl)bis(sulfonyl)]bis[4-meth yl-, (E,E)-

105479-67-2

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Basic information

Product Name: Benzene, 1,1'-[(3,3,4,4-tetramethyl-1,5-hexadiene-1,6-diyl)bis(sulfonyl)]bis[4-meth yl-, (E,E)-
Synonyms:
CAS NO:105479-67-2
Molecular Formula: C24H30O4S2
Molecular Weight: 446.632
EINECS: N/A
Product Categories: N/A
Mol File: 105479-67-2.mol

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: Benzene, 1,1'-[(3,3,4,4-tetramethyl-1,5-hexadiene-1,6-diyl)bis(sulfonyl)]bis[4-meth yl-, (E,E)-(CAS DataBase Reference)
NIST Chemistry Reference: Benzene, 1,1'-[(3,3,4,4-tetramethyl-1,5-hexadiene-1,6-diyl)bis(sulfonyl)]bis[4-meth yl-, (E,E)-(105479-67-2)
EPA Substance Registry System: Benzene, 1,1'-[(3,3,4,4-tetramethyl-1,5-hexadiene-1,6-diyl)bis(sulfonyl)]bis[4-meth yl-, (E,E)-(105479-67-2)

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: 105479-67-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 105479-67-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,4,7 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105479-67:
(8*1)+(7*0)+(6*5)+(5*4)+(4*7)+(3*9)+(2*6)+(1*7)=132
132 % 10 = 2
So 105479-67-2 is a valid CAS Registry Number.

105479-67-2Upstream product

15543-64-3 prenyl tolyl sulfone

105479-67-2Downstream Products

105479-65-0 C₂₄H₃₀O₄S₂

105479-67-2Relevant academic research and scientific papers

OXIDATIVE DIMERIZATION OF ALLYLIC SULFONES WITH IODINE AND WITH FERRIC CHLORIDE

Buechi, G.,Freidinger, Roger M.

, p. 5923 - 5926 (2007/10/02)

Lithium salts of allylic sulfones are oxidized with ferric chloride-dimethylformamide complex mainly to 1,6-disulfones by 3-3' coupling. Products resulting from coupling of 3,3-disubstituted sulfones undergo Cope rearrangements affording vicinal disulfone

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