Cas 136479-92-0,3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,2R,3S)-3-morpholin-4-yl-2-(3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxymethyl)-spiro[3.4]oct-1-ylmethyl ester

136479-92-0

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Basic information

Product Name: 3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,2R,3S)-3-morpholin-4-yl-2-(3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxymethyl)-spiro[3.4]oct-1-ylmethyl ester
Synonyms:
CAS NO:136479-92-0
Molecular Formula:
Molecular Weight: 687.677
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: 3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,2R,3S)-3-morpholin-4-yl-2-(3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxymethyl)-spiro[3.4]oct-1-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,2R,3S)-3-morpholin-4-yl-2-(3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxymethyl)-spiro[3.4]oct-1-ylmethyl ester(136479-92-0)
EPA Substance Registry System: 3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,2R,3S)-3-morpholin-4-yl-2-(3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxymethyl)-spiro[3.4]oct-1-ylmethyl ester(136479-92-0)

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: 136479-92-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 136479-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,4,7 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 136479-92:
(8*1)+(7*3)+(6*6)+(5*4)+(4*7)+(3*9)+(2*9)+(1*2)=160
160 % 10 = 0
So 136479-92-0 is a valid CAS Registry Number.

136479-92-0Upstream product

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136479-92-0Relevant academic research and scientific papers

Asymmetric Reactions of Enamines with Methyl (E)-4-Oxo-4-(2-oxo-1,3-oxazolidin-3-yl)-2-butenoate by Use of a Chiral Titanium Reagent

Hayashi, Yujiro,Otaka, Ken,Saito, Nobuo,Narasaka, Koichi

, p. 2122 - 2127 (2007/10/02)

Asymmetric Michael and cycloaddition reactions between enamines and methyl (E)-4-oxo-4-(2-oxo-1,3-oxazolidin-3-yl)-2-butenoate proceed with a chiral titanium reagent generated in situ from dichlorodiisopropoxytitanium and a tartrate-derived chiral 1,4-diol.In the presence of excess amounts of the chiral titanium reagent, good to moderate enantioselectivity is attained.The reactions are also well catalyzed even with a catalytic amount of the titanium reagent.

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