Cas 165878-01-3,3-(5'-O-benzoyl-2',3'-isopropylidene-β-D-ribofuranos-1'-yl)-5-ethoxycarbonyl-4,5-dihydroisoxazole

165878-01-3

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Basic information

Product Name: 3-(5'-O-benzoyl-2',3'-isopropylidene-β-D-ribofuranos-1'-yl)-5-ethoxycarbonyl-4,5-dihydroisoxazole
Synonyms: 3-(5'-O-benzoyl-2',3'-isopropylidene-β-D-ribofuranos-1'-yl)-5-ethoxycarbonyl-4,5-dihydroisoxazole
CAS NO:165878-01-3
Molecular Formula:
Molecular Weight: 419.431
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-(5'-O-benzoyl-2',3'-isopropylidene-β-D-ribofuranos-1'-yl)-5-ethoxycarbonyl-4,5-dihydroisoxazole(CAS DataBase Reference)
NIST Chemistry Reference: 3-(5'-O-benzoyl-2',3'-isopropylidene-β-D-ribofuranos-1'-yl)-5-ethoxycarbonyl-4,5-dihydroisoxazole(165878-01-3)
EPA Substance Registry System: 3-(5'-O-benzoyl-2',3'-isopropylidene-β-D-ribofuranos-1'-yl)-5-ethoxycarbonyl-4,5-dihydroisoxazole(165878-01-3)

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: 165878-01-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 165878-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,8,7 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 165878-01:
(8*1)+(7*6)+(6*5)+(5*8)+(4*7)+(3*8)+(2*0)+(1*1)=173
173 % 10 = 3
So 165878-01-3 is a valid CAS Registry Number.

165878-01-3Upstream product

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165878-01-3Relevant academic research and scientific papers

Nitrile oxide [3+2] cycloaddition: Application to the synthesis of 6-substituted 3(2H)-pyridazinones and 6-substituted 4,5-dihydro-4-hydroxy-3(2H)-pyridazinones

Baraldi,Bigoni,Cacciari,Caldari,Manfredini,Spalluto

, p. 1158 - 1162 (1994)

An efficient method for the preparation of 6-substituted 3(2H)-pyridazinones and 6-substituted 4,5-dihydro-4-hydroxy-3(2H)-pyridazinones starting from 3,5-disubstituted 4,5-dihydroisoxazoles is described. N-O bond cleavage of the isoxazoline ring promoted

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