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CAS

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934497-20-8

2′-O-benzoyl-3-O-tert-butyldimethylsilyl-L-threonolactone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 934497-20-8 Structure

  • Basic information

    1. Product Name: 2′-O-benzoyl-3-O-tert-butyldimethylsilyl-L-threonolactone
    2. Synonyms: 2′-O-benzoyl-3-O-tert-butyldimethylsilyl-L-threonolactone
    3. CAS NO:934497-20-8
    4. Molecular Formula:
    5. Molecular Weight: 336.46
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 934497-20-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2′-O-benzoyl-3-O-tert-butyldimethylsilyl-L-threonolactone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2′-O-benzoyl-3-O-tert-butyldimethylsilyl-L-threonolactone(934497-20-8)
    11. EPA Substance Registry System: 2′-O-benzoyl-3-O-tert-butyldimethylsilyl-L-threonolactone(934497-20-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 934497-20-8(Hazardous Substances Data)

934497-20-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 934497-20-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,4,4,9 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 934497-20:
(8*9)+(7*3)+(6*4)+(5*4)+(4*9)+(3*7)+(2*2)+(1*0)=198
198 % 10 = 8
So 934497-20-8 is a valid CAS Registry Number.

934497-20-8Relevant articles and documents

Amidate Prodrugs of Deoxythreosyl Nucleoside Phosphonates as Dual Inhibitors of HIV and HBV Replication

Liu, Chao,Dumbre, Shrinivas G.,Pannecouque, Christophe,Huang, Chunsheng,Ptak, Roger G.,Murray, Michael G.,De Jonghe, Steven,Herdewijn, Piet

, p. 9513 - 9531 (2016)

The synthesis of four l-2′-deoxy-threose nucleoside phosphonates with the natural nucleobases adenine, thymine, cytosine, and guanosine has been performed. Especially the adenine containing analogue (PMDTA) was endowed with potent antiviral activity displ

NOVEL ANTIVIRAL COMPOUNDS, A PROCESS FOR THEIR PREPARATION, AND THEIR USE FOR TREATING VIRAL INFECTIONS

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Page/Page column 8; 9; 23, (2017/01/05)

The present invention relates to novel pro-drugs of L-2'-deoxythreose nucleoside phosphonates, such as phosphoramidate, phosphorodiamidate and phospho-diester prodrugs. The invention also relates to a process for preparing these novel prodrugs of nucleoside phosphonates. The invention also relates to the use of these novel phosphonatemodified nucleosides to treat or prevent viral infections and their use to manufacture a medicine to treat or prevent viral infections, particularly infections with viruses belonging to the HBV family.

Synthesis of 3′-O-phosphonomethyl nucleosides with an adenine base moiety

Vi?a, Dolores,Wu, Tongfei,Renders, Marleen,Laflamme, Geneviève,Herdewijn, Piet

, p. 2634 - 2646 (2007/10/03)

A synthetic scheme has been developed for the synthesis of 2′-deoxythreose phosphonate nucleosides from β-hydroxy-γ-butyrolactone and of 2′-azido erythrose phosphonate nucleosides from dihydroxydihydrofuran-1-one. In addition several α-l-arabinofuranose p

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