Cas 1258846-18-2,1-(5-((2S,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)isoxazol-3-yl)ethanone

1258846-18-2

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Basic information

Product Name: 1-(5-((2S,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)isoxazol-3-yl)ethanone
Synonyms:
CAS NO:1258846-18-2
Molecular Formula:
Molecular Weight: 227.217
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: 1-(5-((2S,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)isoxazol-3-yl)ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 1-(5-((2S,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)isoxazol-3-yl)ethanone(1258846-18-2)
EPA Substance Registry System: 1-(5-((2S,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)isoxazol-3-yl)ethanone(1258846-18-2)

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: 1258846-18-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1258846-18-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,8,4 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1258846-18:
(9*1)+(8*2)+(7*5)+(6*8)+(5*8)+(4*4)+(3*6)+(2*1)+(1*8)=192
192 % 10 = 2
So 1258846-18-2 is a valid CAS Registry Number.

1258846-18-2Upstream product

1258846-12-6 1-(5-(4(S)-acetoxy-5(R)-(acetoxymethyl)tetrahydrofuran-2(S)-yl)isoxazol-3-yl)ethanone

1258846-18-2Downstream Products

1258846-18-2Relevant academic research and scientific papers

Alkynyl-2-deoxy-d-riboses, a cornucopia for the generation of families of C-nucleosides

Adamo, Mauro F.A.,Pergoli, Roberto,Moccia, Maria

experimental part, p. 9242 - 9251 (2011/01/12)

This study focuses on the preparation of some 1-alkynyl-2-deoxy-d-riboses and their application to the generation of C-nucleosides analogues. Examples are provided in which the alkyne functionality took part in alkylation or cycloaddition reactions. A discussion of the protecting group used is provided.

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