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852065-42-0

3-isopropoxy-4-vinylbenzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 852065-42-0 Structure

  • Basic information

    1. Product Name: 3-isopropoxy-4-vinylbenzoic acid
    2. Synonyms: 3-isopropoxy-4-vinylbenzoic acid
    3. CAS NO:852065-42-0
    4. Molecular Formula:
    5. Molecular Weight: 206.241
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 852065-42-0.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: 3-isopropoxy-4-vinylbenzoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-isopropoxy-4-vinylbenzoic acid(852065-42-0)
    11. EPA Substance Registry System: 3-isopropoxy-4-vinylbenzoic acid(852065-42-0)

  • 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: 852065-42-0(Hazardous Substances Data)

852065-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 852065-42-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,0,6 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 852065-42:
(8*8)+(7*5)+(6*2)+(5*0)+(4*6)+(3*5)+(2*4)+(1*2)=160
160 % 10 = 0
So 852065-42-0 is a valid CAS Registry Number.

852065-42-0Relevant articles and documents

Terephthalamide derivatives as mimetics of helical peptides: Disruption of the Bcl-xL/Bak interaction

Yin, Hang,Lee, Gui-In,Sedey, Kristine A.,Rodriguez, Johanna M.,Wang, Hong-Gang,Sebti, Said M.,Hamilton, Andrew D.

, p. 5463 - 5468 (2007/10/03)

A series of Bcl-xL/Bak antagonists, based on a terephthalamide scaffold, was designed to mimic the α-helical region of the Bak peptide. These molecules showed favorable in vitro activities in disrupting the Bcl-xL/Bak BH3 domain comp

Terephthalamide derivatives as mimetics of the helical region of Bak peptide target Bcl-xL protein

Yin, Hang,Hamilton, Andrew D.

, p. 1375 - 1379 (2007/10/03)

A group of novel Bcl-xL/Bak antagonists, based on a terephthalamide scaffold, were designed to mimic the α-helical region of the Bak peptide. Good in vitro inhibition potencies in disrupting the Bak/Bcl-xL complex have been observed (terephthalamide 4, K

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