Cas 918332-75-9,(3R,5S,8aR)-5-[(R)-1-(3,5-Bis-trifluoromethyl-phenyl)-ethoxymethyl]-3-phenyl-hexahydro-oxazolo[3,2-a]pyridine-5-carbonitrile

918332-75-9

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Basic information

Product Name: (3R,5S,8aR)-5-[(R)-1-(3,5-Bis-trifluoromethyl-phenyl)-ethoxymethyl]-3-phenyl-hexahydro-oxazolo[3,2-a]pyridine-5-carbonitrile
Synonyms: (3R,5S,8aR)-5-[(R)-1-(3,5-Bis-trifluoromethyl-phenyl)-ethoxymethyl]-3-phenyl-hexahydro-oxazolo[3,2-a]pyridine-5-carbonitrile
CAS NO:918332-75-9
Molecular Formula:
Molecular Weight: 498.468
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: (3R,5S,8aR)-5-[(R)-1-(3,5-Bis-trifluoromethyl-phenyl)-ethoxymethyl]-3-phenyl-hexahydro-oxazolo[3,2-a]pyridine-5-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (3R,5S,8aR)-5-[(R)-1-(3,5-Bis-trifluoromethyl-phenyl)-ethoxymethyl]-3-phenyl-hexahydro-oxazolo[3,2-a]pyridine-5-carbonitrile(918332-75-9)
EPA Substance Registry System: (3R,5S,8aR)-5-[(R)-1-(3,5-Bis-trifluoromethyl-phenyl)-ethoxymethyl]-3-phenyl-hexahydro-oxazolo[3,2-a]pyridine-5-carbonitrile(918332-75-9)

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: 918332-75-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 918332-75-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,3,3 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 918332-75:
(8*9)+(7*1)+(6*8)+(5*3)+(4*3)+(3*2)+(2*7)+(1*5)=179
179 % 10 = 9
So 918332-75-9 is a valid CAS Registry Number.

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918332-75-9Relevant academic research and scientific papers

Two complementary, diversity-driven asymmetric syntheses of a 2,2-disubstituted piperidine NK1 antagonist

Xiao, Dong,Wang, Cheng,Palani, Anandan,Reichard, Gregory,Aslanian, Robert,Shih, Neng-Yang,Buevich, Alexei

, p. 2596 - 2598 (2006)

Two diversity-driven asymmetric syntheses of a potent NK1 receptor antagonist 1 were achieved. These syntheses provided two complementary approaches that were well positioned for further modifications of several different sites of medicinal che

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