Cas 145679-80-7,(R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-thiopropionic acid S-(3'-methyl-1',4'-diphenyl-[1,2']binaphthalenyl-8-yl) ester

145679-80-7

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Basic information

Product Name: (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-thiopropionic acid S-(3'-methyl-1',4'-diphenyl-[1,2']binaphthalenyl-8-yl) ester
Synonyms:
CAS NO:145679-80-7
Molecular Formula:
Molecular Weight: 668.779
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: (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-thiopropionic acid S-(3'-methyl-1',4'-diphenyl-[1,2']binaphthalenyl-8-yl) ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-thiopropionic acid S-(3'-methyl-1',4'-diphenyl-[1,2']binaphthalenyl-8-yl) ester(145679-80-7)
EPA Substance Registry System: (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-thiopropionic acid S-(3'-methyl-1',4'-diphenyl-[1,2']binaphthalenyl-8-yl) ester(145679-80-7)

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: 145679-80-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 145679-80-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,6,7 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 145679-80:
(8*1)+(7*4)+(6*5)+(5*6)+(4*7)+(3*9)+(2*8)+(1*0)=167
167 % 10 = 7
So 145679-80-7 is a valid CAS Registry Number.

145679-80-7Upstream product

145679-80-7Downstream Products

145627-15-2 3'-Methyl-1',4'-diphenyl-[1,2']binaphthalenyl-8-thiol

145679-80-7Relevant academic research and scientific papers

Synthesis of a Chiral Binaphthyldisulfide: A Potentially Useful Reagent for Catalytic Asymmetric Synthesis

Feldman, Ken S.,Ruckle, Robert E.,Ensel, Susan M.,Weinreb, Paul H.

, p. 7101 - 7102 (1992)

Diels Alder cycloaddition/oxygen-atom-extrusion provides the means to unite two naphthylene fragments and affords a highly functionalized, racemic binaphthyl iodide.Resolution of a derived thiol then furnishes, after appropriate manipulation, enantiomeric

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