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CAS

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34311-67-6

3-deoxy-3-(hydroxymethyl)-1,2-O-(1-methylethylidene)-5-O-(phenylmethyl)-α-D-ribofuranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 34311-67-6 Structure

  • Basic information

    1. Product Name: 3-deoxy-3-(hydroxymethyl)-1,2-O-(1-methylethylidene)-5-O-(phenylmethyl)-α-D-ribofuranose
    2. Synonyms: 3-deoxy-3-(hydroxymethyl)-1,2-O-(1-methylethylidene)-5-O-(phenylmethyl)-α-D-ribofuranose
    3. CAS NO:34311-67-6
    4. Molecular Formula:
    5. Molecular Weight: 294.348
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 34311-67-6.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: 3-deoxy-3-(hydroxymethyl)-1,2-O-(1-methylethylidene)-5-O-(phenylmethyl)-α-D-ribofuranose(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-deoxy-3-(hydroxymethyl)-1,2-O-(1-methylethylidene)-5-O-(phenylmethyl)-α-D-ribofuranose(34311-67-6)
    11. EPA Substance Registry System: 3-deoxy-3-(hydroxymethyl)-1,2-O-(1-methylethylidene)-5-O-(phenylmethyl)-α-D-ribofuranose(34311-67-6)

  • 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: 34311-67-6(Hazardous Substances Data)

34311-67-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34311-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,3,1 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34311-67:
(7*3)+(6*4)+(5*3)+(4*1)+(3*1)+(2*6)+(1*7)=86
86 % 10 = 6
So 34311-67-6 is a valid CAS Registry Number.

34311-67-6Relevant articles and documents

Synthesis and antiviral activity of novel isonucleoside analogs

Tino,Clark,Field,Jacobs,Lis,Michalik,McGeever-Rubin,Slusarchyk,Spergel,Sundeen,Tuomari,Weaver,Young,Zahler

, p. 1221 - 1229 (1993)

A series of branched-chain sugar isonucleosides was synthesized and evaluated for antiviral activity against herpesviruses. The preparation of homochiral [3S-(3α,4β,5α)]-2-amino-1,9-dihydro-9-[tetrahydro-4,5- bis(hydroxymethyl)-3-furanyl]-6H-purin-6-one (

3′-C-branched-chain-substituted nucleosides and nucleotides as potent inhibitors of Mycobacterium tuberculosis thymidine monophosphate kinase

Vanheusden, Veerle,Munier-Lehmann, Hélène,Froeyen, Matheus,Dugué, Laurence,Heyerick, Arne,De Keukeleire, Denis,Pochet, Sylvie,Busson, Roger,Herdewijn, Piet,Van Calenbergh, Serge

, p. 3811 - 3821 (2007/10/03)

Thymidine monophosphate kinase (TMPK) of Mycobacterium tuberculosis (TMPKmt) represents an attractive target for blocking the bacterial DNA synthesis. In an attempt to find high-affinity inhibitors of TMPKmt, a cavity in the enzyme at the 3′-position was

Purinyl tetrahydrofurans

-

, (2008/06/13)

Antiviral activity is exhibited by compounds having the formula STR1 and pharmaceutically acceptable salts thereof wherein R1 is a purine or pyrimidine base or an analog thereof and R2 and R3 are independently hydrogen, --

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