Cas 935265-36-4,1-(4-(2-(1-(tert-butyldimethylsilyloxy)-7-phenylheptyl)oxazol-5-yl)phenyl)-2,2,2-trifluoroethanone

935265-36-4

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Basic information

Product Name: 1-(4-(2-(1-(tert-butyldimethylsilyloxy)-7-phenylheptyl)oxazol-5-yl)phenyl)-2,2,2-trifluoroethanone
Synonyms: 1-(4-(2-(1-(tert-butyldimethylsilyloxy)-7-phenylheptyl)oxazol-5-yl)phenyl)-2,2,2-trifluoroethanone
CAS NO:935265-36-4
Molecular Formula:
Molecular Weight: 545.717
EINECS: N/A
Product Categories: N/A
Mol File: 935265-36-4.mol
Article Data: 2

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: 1-(4-(2-(1-(tert-butyldimethylsilyloxy)-7-phenylheptyl)oxazol-5-yl)phenyl)-2,2,2-trifluoroethanone(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-(2-(1-(tert-butyldimethylsilyloxy)-7-phenylheptyl)oxazol-5-yl)phenyl)-2,2,2-trifluoroethanone(935265-36-4)
EPA Substance Registry System: 1-(4-(2-(1-(tert-butyldimethylsilyloxy)-7-phenylheptyl)oxazol-5-yl)phenyl)-2,2,2-trifluoroethanone(935265-36-4)

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: 935265-36-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 935265-36-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,5,2,6 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 935265-36:
(8*9)+(7*3)+(6*5)+(5*2)+(4*6)+(3*5)+(2*3)+(1*6)=184
184 % 10 = 4
So 935265-36-4 is a valid CAS Registry Number.

935265-36-4Upstream product

935265-36-4Downstream Products

935265-36-4Relevant articles and documents

Oxazole ketones as modulators of fatty acid amide hydrolase

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Page/Page column 11-12, (2008/06/13)

Certain oxazole ketone compounds are useful as FAAH inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by fatty acid amide hydrolase (FAAH) activity. Th

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