Cas 53641-69-3,2-ethyl-6-[O2,O3-isopropylidene-O5-(toluene-4-sulfonyl)-β-D-ribofuranosyl]-6H-oxazolo[5,4-d]pyrimidin-7-one

53641-69-3

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Basic information

Product Name: 2-ethyl-6-[O²,O³-isopropylidene-O⁵-(toluene-4-sulfonyl)-β-D-ribofuranosyl]-6H-oxazolo[5,4-d]pyrimidin-7-one
Synonyms:
CAS NO:53641-69-3
Molecular Formula:
Molecular Weight: 491.522
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: 2-ethyl-6-[O²,O³-isopropylidene-O⁵-(toluene-4-sulfonyl)-β-D-ribofuranosyl]-6H-oxazolo[5,4-d]pyrimidin-7-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-ethyl-6-[O²,O³-isopropylidene-O⁵-(toluene-4-sulfonyl)-β-D-ribofuranosyl]-6H-oxazolo[5,4-d]pyrimidin-7-one(53641-69-3)
EPA Substance Registry System: 2-ethyl-6-[O²,O³-isopropylidene-O⁵-(toluene-4-sulfonyl)-β-D-ribofuranosyl]-6H-oxazolo[5,4-d]pyrimidin-7-one(53641-69-3)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 53641-69-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 53641-69-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,4 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53641-69:
(7*5)+(6*3)+(5*6)+(4*4)+(3*1)+(2*6)+(1*9)=123
123 % 10 = 3
So 53641-69-3 is a valid CAS Registry Number.

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53641-69-3Relevant academic research and scientific papers

Synthesis and biological activity of selected 2 substituted 6 (β D ribofuranosyl)oxazolo[5,4 d]pyrimidin 7 ones

Patil,Wise,Townsend,Bloch

, p. 1282 - 1285 (2007/10/09)

Several 2 substituted 6 (β D ribofuranosyl)oxazolo[5,4 d]pyrimidin 7 ones were prepared by condensation of the appropriate silylated heterocyles with 2,3,5 tri O acetyl β D ribofuranosyl bromide and the subsequent removal of blocking groups from the carbo

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