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171569-35-0

1,3-Dimethoxy-5-non-8-ynyl-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 171569-35-0 Structure

  • Basic information

    1. Product Name: 1,3-Dimethoxy-5-non-8-ynyl-benzene
    2. Synonyms: 1,3-Dimethoxy-5-non-8-ynyl-benzene
    3. CAS NO:171569-35-0
    4. Molecular Formula:
    5. Molecular Weight: 260.376
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 171569-35-0.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: 1,3-Dimethoxy-5-non-8-ynyl-benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-Dimethoxy-5-non-8-ynyl-benzene(171569-35-0)
    11. EPA Substance Registry System: 1,3-Dimethoxy-5-non-8-ynyl-benzene(171569-35-0)

  • 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: 171569-35-0(Hazardous Substances Data)

171569-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 171569-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,5,6 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 171569-35:
(8*1)+(7*7)+(6*1)+(5*5)+(4*6)+(3*9)+(2*3)+(1*5)=150
150 % 10 = 0
So 171569-35-0 is a valid CAS Registry Number.

171569-35-0Relevant articles and documents

5-Alkylresorcinols from Hakea trifurcata that cleave DNA

Lytollis, William,Scannell, Ralph T.,An, Haoyun,Murty,Reddy, K. Sambi,Barr, John R.,Hecht, Sidney M.

, p. 12683 - 12690 (1995)

A dichloromethane extract of Hakea trifurcata that mediated relaxation of ?X174 replicative form DNA at micromolar concentrations in the presence of Cu2+ was resolved into six active components by bioassay-guided fractionation. Five of the acti

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