Cas 94371-26-3,5-[(1R,2R)-2-(tert-Butyl-dimethyl-silanyloxy)-cyclohexylmethyl]-3-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-isoxazole

94371-26-3

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Basic information

Product Name: 5-[(1R,2R)-2-(tert-Butyl-dimethyl-silanyloxy)-cyclohexylmethyl]-3-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-isoxazole
Synonyms: 5-[(1R,2R)-2-(tert-Butyl-dimethyl-silanyloxy)-cyclohexylmethyl]-3-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-isoxazole
CAS NO:94371-26-3
Molecular Formula:
Molecular Weight: 423.668
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: 5-[(1R,2R)-2-(tert-Butyl-dimethyl-silanyloxy)-cyclohexylmethyl]-3-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-isoxazole(CAS DataBase Reference)
NIST Chemistry Reference: 5-[(1R,2R)-2-(tert-Butyl-dimethyl-silanyloxy)-cyclohexylmethyl]-3-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-isoxazole(94371-26-3)
EPA Substance Registry System: 5-[(1R,2R)-2-(tert-Butyl-dimethyl-silanyloxy)-cyclohexylmethyl]-3-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-isoxazole(94371-26-3)

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: 94371-26-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 94371-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,3,7 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 94371-26:
(7*9)+(6*4)+(5*3)+(4*7)+(3*1)+(2*2)+(1*6)=143
143 % 10 = 3
So 94371-26-3 is a valid CAS Registry Number.

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94371-26-3Relevant academic research and scientific papers

A Nitrile Oxide Based Entry to 2,3-Dihydropyran-4-ones. Synthesis of a Protected Version of "Compactin Lactone" in Racemic and Optically Active Forms

Kozikowski, Alan P.,Li, Chun-Sing

, p. 778 - 785 (2007/10/02)

The use of nitrile oxides bearing a masked β-oxo group as β-hydroxy-3-oxopropionylating agents for the vicinal functionalization of olefins is described.The β-hydroxy ketones revealed on hydrogenation of the initially formed 1,3-dipolar cycloaddition prod

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