Cas 139050-56-9,(R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (R)-2,2,2-trifluoro-1-(2,4,6-trimethyl-phenyl)-ethyl ester

139050-56-9

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Basic information

Product Name: (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (R)-2,2,2-trifluoro-1-(2,4,6-trimethyl-phenyl)-ethyl ester
Synonyms: (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (R)-2,2,2-trifluoro-1-(2,4,6-trimethyl-phenyl)-ethyl ester
CAS NO:139050-56-9
Molecular Formula:
Molecular Weight: 434.378
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-propionic acid (R)-2,2,2-trifluoro-1-(2,4,6-trimethyl-phenyl)-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (R)-2,2,2-trifluoro-1-(2,4,6-trimethyl-phenyl)-ethyl ester(139050-56-9)
EPA Substance Registry System: (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (R)-2,2,2-trifluoro-1-(2,4,6-trimethyl-phenyl)-ethyl ester(139050-56-9)

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: 139050-56-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 139050-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,0,5 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 139050-56:
(8*1)+(7*3)+(6*9)+(5*0)+(4*5)+(3*0)+(2*5)+(1*6)=119
119 % 10 = 9
So 139050-56-9 is a valid CAS Registry Number.

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139050-56-9Relevant academic research and scientific papers

Remarkably effective and simple syntheses of enantiomerically pure secondary carbinols from achiral ketones

Corey,Cheng,Cimprich,Sarshar

, p. 6835 - 6838 (1991)

The chiral oxazaborolidine (1)-catalyzed reduction of the ketones 2, 6 and 8 has provided simple access to the chiral secondary carbinols 3, 7, and 9 in very high enantiomeric purity.

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