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126638-03-7

α-N6-benzyl-2',3'-dideoxyadenosine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126638-03-7 Structure

  • Basic information

    1. Product Name: α-N6-benzyl-2',3'-dideoxyadenosine
    2. Synonyms: α-N6-benzyl-2',3'-dideoxyadenosine
    3. CAS NO:126638-03-7
    4. Molecular Formula:
    5. Molecular Weight: 325.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126638-03-7.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: α-N6-benzyl-2',3'-dideoxyadenosine(CAS DataBase Reference)
    10. NIST Chemistry Reference: α-N6-benzyl-2',3'-dideoxyadenosine(126638-03-7)
    11. EPA Substance Registry System: α-N6-benzyl-2',3'-dideoxyadenosine(126638-03-7)

  • 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: 126638-03-7(Hazardous Substances Data)

126638-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126638-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,6,3 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 126638-03:
(8*1)+(7*2)+(6*6)+(5*6)+(4*3)+(3*8)+(2*0)+(1*3)=127
127 % 10 = 7
So 126638-03-7 is a valid CAS Registry Number.

126638-03-7Downstream Products

126638-03-7Relevant articles and documents

Synthesis and Structure-Activity Relationships of 6-Substituted 2',3'-Dideoxypurine Nucleosides as Potential Anti-Human Immunodeficiency Virus Agents

Chu, Chung K.,Ullas, Giliyar V.,Jeong, Lak S.,Ahn, Soon K.,Doboszewski, Bogdan,et al.

, p. 1553 - 1561 (2007/10/02)

In order to study the structure-activity relationships of 2',3'-dideoxypurine nucleosides as potential anti-HIV agents, various 6-substituted purine analogues have been synthesized and examined in virus-infected and uninfected human peripheral blood monon

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