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1229622-80-3

C42H47N5O6 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1229622-80-3 Structure

  • Basic information

    1. Product Name: C42H47N5O6
    2. Synonyms: C42H47N5O6
    3. CAS NO:1229622-80-3
    4. Molecular Formula:
    5. Molecular Weight: 717.865
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1229622-80-3.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: C42H47N5O6(CAS DataBase Reference)
    10. NIST Chemistry Reference: C42H47N5O6(1229622-80-3)
    11. EPA Substance Registry System: C42H47N5O6(1229622-80-3)

  • 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: 1229622-80-3(Hazardous Substances Data)

1229622-80-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1229622-80-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,9,6,2 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1229622-80:
(9*1)+(8*2)+(7*2)+(6*9)+(5*6)+(4*2)+(3*2)+(2*8)+(1*0)=153
153 % 10 = 3
So 1229622-80-3 is a valid CAS Registry Number.

1229622-80-3Downstream Products

1229622-80-3Relevant articles and documents

Regioselective alkylation of the exocyclic nitrogen of adenine and adenosine by the Mitsunobu reaction

Fletcher, Steven

experimental part, p. 2948 - 2950 (2010/06/21)

A novel synthetic route to N6-substitution of adenine is presented, employing the Mitsunobu reaction as the key step. A range of primary and secondary alcohols all coupled in very good to excellent yields within 30 min at 45 °C, offering a milder alternative to the traditional nucleophilic aromatic substitution of 6-chloropurine. The utility of this protocol is further demonstrated by its application to the syntheses of N6,N9-di-substituted adenines, including the potent and selective A1 adenosine receptor agonist N6-cyclopentyladenosine.

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