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129852-17-1

{3-[4-(Quinolin-2-ylmethoxy)-phenyl]-cyclopentyl}-acetic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 129852-17-1 Structure

  • Basic information

    1. Product Name: {3-[4-(Quinolin-2-ylmethoxy)-phenyl]-cyclopentyl}-acetic acid methyl ester
    2. Synonyms:
    3. CAS NO:129852-17-1
    4. Molecular Formula:
    5. Molecular Weight: 375.467
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 129852-17-1.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: {3-[4-(Quinolin-2-ylmethoxy)-phenyl]-cyclopentyl}-acetic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: {3-[4-(Quinolin-2-ylmethoxy)-phenyl]-cyclopentyl}-acetic acid methyl ester(129852-17-1)
    11. EPA Substance Registry System: {3-[4-(Quinolin-2-ylmethoxy)-phenyl]-cyclopentyl}-acetic acid methyl ester(129852-17-1)

  • 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: 129852-17-1(Hazardous Substances Data)

129852-17-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129852-17-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,8,5 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129852-17:
(8*1)+(7*2)+(6*9)+(5*8)+(4*5)+(3*2)+(2*1)+(1*7)=151
151 % 10 = 1
So 129852-17-1 is a valid CAS Registry Number.

129852-17-1Relevant articles and documents

The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency

Galemmo Jr.,Johnson Jr.,Learn,Lee,Huang,Campbell,Youssefyeh,O'Rourke,Schuessler,Sweeney,Travis,Sutherland,Nuss,Carnathan,Van Inwegen

, p. 2828 - 2841 (2007/10/02)

This paper is the third in a series outlining the development of orally active sulfido peptide leukotriene antagonists containing a (quinolin-2-ylmethoxy)phenyl moiety. In this work the systematic variation of the acid side chain substituents led to drama

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