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CAS

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652173-18-7

9-benzyl-6-(4'-azido-4'-deoxy-β-L-rhamnopyranosylamino)-9H-purine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 652173-18-7 Structure

  • Basic information

    1. Product Name: 9-benzyl-6-(4'-azido-4'-deoxy-β-L-rhamnopyranosylamino)-9H-purine
    2. Synonyms: 9-benzyl-6-(4'-azido-4'-deoxy-β-L-rhamnopyranosylamino)-9H-purine
    3. CAS NO:652173-18-7
    4. Molecular Formula:
    5. Molecular Weight: 396.409
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 652173-18-7.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: 9-benzyl-6-(4'-azido-4'-deoxy-β-L-rhamnopyranosylamino)-9H-purine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9-benzyl-6-(4'-azido-4'-deoxy-β-L-rhamnopyranosylamino)-9H-purine(652173-18-7)
    11. EPA Substance Registry System: 9-benzyl-6-(4'-azido-4'-deoxy-β-L-rhamnopyranosylamino)-9H-purine(652173-18-7)

  • 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: 652173-18-7(Hazardous Substances Data)

652173-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 652173-18-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,2,1,7 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 652173-18:
(8*6)+(7*5)+(6*2)+(5*1)+(4*7)+(3*3)+(2*1)+(1*8)=147
147 % 10 = 7
So 652173-18-7 is a valid CAS Registry Number.

652173-18-7Upstream product

652173-18-7Relevant articles and documents

An approach to the generation of simple analogues of the antitumour agent spicamycin.

Mons, Stephane,Fleet, George W J

, p. 3685 - 3691 (2003)

The one-step glycosylation of arylamines in acidic medium is extended to adenine derivatives for the first time, providing a considerable improvement over existing reactions. This method is used to prepare some rhamnospicamycin analogues containing differ

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