Cas 84987-88-2,3-[(3aS,4S,6R,6aR)-6-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-5-phenyl-4,5-dihydro-isoxazole

84987-88-2

Post Buying Request

Basic information

Product Name: 3-[(3aS,4S,6R,6aR)-6-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-5-phenyl-4,5-dihydro-isoxazole
Synonyms:
CAS NO:84987-88-2
Molecular Formula:
Molecular Weight: 433.62
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-[(3aS,4S,6R,6aR)-6-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-5-phenyl-4,5-dihydro-isoxazole(CAS DataBase Reference)
NIST Chemistry Reference: 3-[(3aS,4S,6R,6aR)-6-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-5-phenyl-4,5-dihydro-isoxazole(84987-88-2)
EPA Substance Registry System: 3-[(3aS,4S,6R,6aR)-6-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-5-phenyl-4,5-dihydro-isoxazole(84987-88-2)

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: 84987-88-2(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

84987-88-2 Suppliers

Recommended suppliers

84987-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84987-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,8 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 84987-88:
(7*8)+(6*4)+(5*9)+(4*8)+(3*7)+(2*8)+(1*8)=202
202 % 10 = 2
So 84987-88-2 is a valid CAS Registry Number.

84987-88-2Upstream product

84987-88-2Downstream Products

84987-88-2Relevant academic research and scientific papers

The Nitrile Oxide Cycloaddition (NOC) Route to a Multipurpose C-Nucleoside Intermediate: A New Class of C-Nucleosides

Kozikowski, Alan P.,Goldstein, Steven

, p. 1139 - 1141 (1983)

A new route to the important class of antibiotic and antiviral agents, the C-nucleosides, has been developed.The nitrile oxide generated from a protected derivative of β-D-ribofuranosylnitromethane has been shown to react with ethoxyacetylene to deliver an isoxazole C-nucleoside.On hydrogenolytic cleavage of the N-O bond, a β-keto ester is formed that can be reacted with a bisnucleophile to yield a new C-nucleoside analogue.

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

What can I do for you?
Get Best Price

Get Best Price for 84987-88-2