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9H-Purin-6-amine, 9-[3-(triphenylmethoxy)-1-propenyl]-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156518-69-3 Structure
  • Basic information

    1. Product Name: 9H-Purin-6-amine, 9-[3-(triphenylmethoxy)-1-propenyl]-, (Z)-
    2. Synonyms:
    3. CAS NO:156518-69-3
    4. Molecular Formula: C27H23N5O
    5. Molecular Weight: 433.513
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156518-69-3.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: 9H-Purin-6-amine, 9-[3-(triphenylmethoxy)-1-propenyl]-, (Z)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9H-Purin-6-amine, 9-[3-(triphenylmethoxy)-1-propenyl]-, (Z)-(156518-69-3)
    11. EPA Substance Registry System: 9H-Purin-6-amine, 9-[3-(triphenylmethoxy)-1-propenyl]-, (Z)-(156518-69-3)
  • 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: 156518-69-3(Hazardous Substances Data)

156518-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156518-69-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,5,1 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 156518-69:
(8*1)+(7*5)+(6*6)+(5*5)+(4*1)+(3*8)+(2*6)+(1*9)=153
153 % 10 = 3
So 156518-69-3 is a valid CAS Registry Number.

156518-69-3Downstream Products

156518-69-3Relevant articles and documents

Synthesis and antiherpetic activity of (Z)- and (E)-9-(3- Phosphonomethoxyprop-1-en-yl)adenines

Ivanov,Andronova,Galegov,Jasko

, p. 58 - 65 (2008/02/01)

The isomeric (Z)- and (E)-9-(3-phosphonomethoxyprop-1-en-yl)adenines were synthesized. The stereoselectivity of double bond formation was studied by variation of sulfonyl groups. The resulting phosphonates exhibited a moderate antiherpetic activity in a c

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