Cas 859911-68-5,(4'S,5'S)-4',5'-diphenyl-1',3'-dioxolane-spiro[2'.6]-5,6-dihydro-7H-1,3-dithiolo[4,5-b]-1,4-dithiepin-2-one

859911-68-5

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Basic information

Product Name: (4'S,5'S)-4',5'-diphenyl-1',3'-dioxolane-spiro[2'.6]-5,6-dihydro-7H-1,3-dithiolo[4,5-b]-1,4-dithiepin-2-one
Synonyms: (4'S,5'S)-4',5'-diphenyl-1',3'-dioxolane-spiro[2'.6]-5,6-dihydro-7H-1,3-dithiolo[4,5-b]-1,4-dithiepin-2-one
CAS NO:859911-68-5
Molecular Formula:
Molecular Weight: 432.609
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: (4'S,5'S)-4',5'-diphenyl-1',3'-dioxolane-spiro[2'.6]-5,6-dihydro-7H-1,3-dithiolo[4,5-b]-1,4-dithiepin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (4'S,5'S)-4',5'-diphenyl-1',3'-dioxolane-spiro[2'.6]-5,6-dihydro-7H-1,3-dithiolo[4,5-b]-1,4-dithiepin-2-one(859911-68-5)
EPA Substance Registry System: (4'S,5'S)-4',5'-diphenyl-1',3'-dioxolane-spiro[2'.6]-5,6-dihydro-7H-1,3-dithiolo[4,5-b]-1,4-dithiepin-2-one(859911-68-5)

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: 859911-68-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 859911-68-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,9,9,1 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 859911-68:
(8*8)+(7*5)+(6*9)+(5*9)+(4*1)+(3*1)+(2*6)+(1*8)=225
225 % 10 = 5
So 859911-68-5 is a valid CAS Registry Number.

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859911-68-5Relevant academic research and scientific papers

Synthetic strategies to chiral organosulfur donors related to bis(ethylenedithio)tetrathiafulvalene

Griffiths, Jon-Paul,Nie, Hui,Brown, R. James,Day, Peter,Wallis, John D.

, p. 2155 - 2166 (2005)

Syntheses of enantiopure organosulfur donors by three different strategies requiring only four-six steps are reported. The key step involves either double substitution of an enantiopure cyclic sulfate ester by a dithiolate, attachment of a chiral diol as

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