Cas 250699-03-7,(+)-β-D-carbocyclic-1'-(1H-[N<sup>3</sup>-benzyloxymethyl]-thymin-1-yl)-2',3'-O-isopropylidene-5'-O-(tert-butyldimethylsilyl) ribonucleoside

250699-03-7

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Basic information

Product Name: (+)-β-D-carbocyclic-1'-(1H-[N³-benzyloxymethyl]-thymin-1-yl)-2',3'-O-isopropylidene-5'-O-(tert-butyldimethylsilyl) ribonucleoside
Synonyms: (+)-β-D-carbocyclic-1'-(1H-[N³-benzyloxymethyl]-thymin-1-yl)-2',3'-O-isopropylidene-5'-O-(tert-butyldimethylsilyl) ribonucleoside
CAS NO:250699-03-7
Molecular Formula:
Molecular Weight: 530.737
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: (+)-β-D-carbocyclic-1'-(1H-[N³-benzyloxymethyl]-thymin-1-yl)-2',3'-O-isopropylidene-5'-O-(tert-butyldimethylsilyl) ribonucleoside(CAS DataBase Reference)
NIST Chemistry Reference: (+)-β-D-carbocyclic-1'-(1H-[N³-benzyloxymethyl]-thymin-1-yl)-2',3'-O-isopropylidene-5'-O-(tert-butyldimethylsilyl) ribonucleoside(250699-03-7)
EPA Substance Registry System: (+)-β-D-carbocyclic-1'-(1H-[N³-benzyloxymethyl]-thymin-1-yl)-2',3'-O-isopropylidene-5'-O-(tert-butyldimethylsilyl) ribonucleoside(250699-03-7)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 250699-03-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 250699-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,0,6,9 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 250699-03:
(8*2)+(7*5)+(6*0)+(5*6)+(4*9)+(3*9)+(2*0)+(1*3)=147
147 % 10 = 7
So 250699-03-7 is a valid CAS Registry Number.

250699-03-7Upstream product

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250699-03-7Relevant academic research and scientific papers

Synthesis of chiral carbocyclic ribonucleotides

Antle, Vincent D.,Caperelli, Carol A.

, p. 1911 - 1928 (1999)

The carbocyclic analogs of CMP, UMP, GMP, IMP, and ribo-TMP, of the same absolute configuration as the naturally occurring β-D-ribofuranose-based ribonucleoside monophosphates, have been synthesized. The synthetic route employed Mitsunobu coupling of the

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