Cas 401515-26-2,{3-[3-(<i>tert</i>-butyl-dimethyl-silanyloxy)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-5-methyl-2,6-dioxo-3,6-dihydro-2<i>H</i>-pyrimidin-1-yl}-acetic acid benzyl ester

401515-26-2

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Basic information

Product Name: {3-[3-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-5-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl}-acetic acid benzyl ester
Synonyms:
CAS NO:401515-26-2
Molecular Formula:
Molecular Weight: 520.655
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-[3-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-5-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl}-acetic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {3-[3-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-5-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl}-acetic acid benzyl ester(401515-26-2)
EPA Substance Registry System: {3-[3-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-5-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl}-acetic acid benzyl ester(401515-26-2)

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: 401515-26-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 401515-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,1,5,1 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 401515-26:
(8*4)+(7*0)+(6*1)+(5*5)+(4*1)+(3*5)+(2*2)+(1*6)=92
92 % 10 = 2
So 401515-26-2 is a valid CAS Registry Number.

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401515-26-2Relevant academic research and scientific papers

Identification of a novel family of nucleosides that specifically inhibit HIV-1 reverse transcriptase

Chamorro, Cristina,Lobaton, Esther,Bonache, Maria-Cruz,De Clercq, Erik,Balzarini, Jan,Velazquez, Sonsoles,San-Felix, Ana,Camarasa, Maria-Jose

, p. 3085 - 3088 (2007/10/03)

N-3-Benzyloxycarbonylmethyl- and N-3-carboxymethyl-TBDMS-substituted nucleosides were synthesized and evaluated for activity against HIV replication. It was found that the N-3-carboxymethyl-TBDMS-substituted nucleosides were specific inhibitors of HIV-1 replication. They should be considered as members of a novel and original class of NNRTIs.

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