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CAS

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1315092-34-2

5'-O-tert-butyldiphenylsilyl-2',3'-didehydro-2',3'-dideoxy-4'-methoxyadenosine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1315092-34-2 Structure

  • Basic information

    1. Product Name: 5'-O-tert-butyldiphenylsilyl-2',3'-didehydro-2',3'-dideoxy-4'-methoxyadenosine
    2. Synonyms:
    3. CAS NO:1315092-34-2
    4. Molecular Formula:
    5. Molecular Weight: 501.66
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1315092-34-2.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: 5'-O-tert-butyldiphenylsilyl-2',3'-didehydro-2',3'-dideoxy-4'-methoxyadenosine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5'-O-tert-butyldiphenylsilyl-2',3'-didehydro-2',3'-dideoxy-4'-methoxyadenosine(1315092-34-2)
    11. EPA Substance Registry System: 5'-O-tert-butyldiphenylsilyl-2',3'-didehydro-2',3'-dideoxy-4'-methoxyadenosine(1315092-34-2)

  • 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: 1315092-34-2(Hazardous Substances Data)

1315092-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1315092-34-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,0,9 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1315092-34:
(9*1)+(8*3)+(7*1)+(6*5)+(5*0)+(4*9)+(3*2)+(2*3)+(1*4)=122
122 % 10 = 2
So 1315092-34-2 is a valid CAS Registry Number.

1315092-34-2Upstream product

1315092-34-2Downstream Products

1315092-34-2Relevant articles and documents

A Ferrier-type allylic rearrangement of 3′-deoxy-3′,4′- didehydronucleosides mediated by DMF dimethyl acetal: Direct access to 4′-alkoxy-2′,3′-didehydro-2′,3′-dideoxynucleosides

Petrova, Magdalena,Budesinsky, Milos,Zbornikova, Eva,Fiedler, Pavel,Rosenberg, Ivan

, p. 4200 - 4203 (2011)

A straightforward synthesis of epimeric 4′-alkoxy-substituted 2′,3′-didehydro-2′,3′-dideoxynucleosides via a DMF dimethyl acetal mediated allylic rearrangement of 3′-deoxy-3′, 4′-didehydronucleosides is described.

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