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CAS

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887604-05-9

((pentadec-14-yn-1-yloxy)methyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 887604-05-9 Structure

  • Basic information

    1. Product Name: ((pentadec-14-yn-1-yloxy)methyl)benzene
    2. Synonyms: ((pentadec-14-yn-1-yloxy)methyl)benzene
    3. CAS NO:887604-05-9
    4. Molecular Formula:
    5. Molecular Weight: 314.511
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 887604-05-9.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: ((pentadec-14-yn-1-yloxy)methyl)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: ((pentadec-14-yn-1-yloxy)methyl)benzene(887604-05-9)
    11. EPA Substance Registry System: ((pentadec-14-yn-1-yloxy)methyl)benzene(887604-05-9)

  • 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: 887604-05-9(Hazardous Substances Data)

887604-05-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 887604-05-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,6,0 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 887604-05:
(8*8)+(7*8)+(6*7)+(5*6)+(4*0)+(3*4)+(2*0)+(1*5)=209
209 % 10 = 9
So 887604-05-9 is a valid CAS Registry Number.

887604-05-9Relevant articles and documents

NUCLEOSIDE PRODRUGS AND USES RELATED THERETO

-

, (2021/02/26)

Disclosed are acyclic nucleoside prodrugs with improved metabolic stability and oral bioavailability. In general, the prodrugs are derivatives of acyclic nucleoside phosphonates containing a lipid-like moiety that can increase oral absorption and subsequent stability in the liver and plasma. Preferably, the lipid-like moiety can resist enzyme-mediated ω-oxidation, such as ω -oxidation catalyzed by cytochrome P450 enzymes. Also disclosed are pharmaceutical formulations of the acyclic nucleoside prodrugs. The acyclic nucleoside prodrugs and pharmaceutical formulations thereof can be used to treat viral infections, such as HIV infections, and/or viral-associated cancer, such as HPV-associated cancers.

Quinol fatty alcohols as promoters of axonal growth

Hanbali, Mazen,Vela-Ruiz, Marta,Bagnard, Dominique,Luu, Bang

, p. 2637 - 2640 (2007/10/03)

The synthesis of three series of quinol fatty alcohols (QFAs) and their biological activities on the promotion of axonal growth are described. Interestingly, the 15-(2,5-dimethoxyphenyl)pentadecan-1-ol, the QFA bearing 15 carbon atoms on the side chain (n = 15), shows the most potent promotion of axonal growth in the presence of both permissive and non-permissive naturally occurring substrates such as Sema3A and myelin proteins.

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