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L-Alanine, N-[4-ethenyl-3-(1-methylethoxy)benzoyl]-N-(2-methylpropyl)-, 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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  • 681465-96-3 Structure
  • Basic information

    1. Product Name: L-Alanine, N-[4-ethenyl-3-(1-methylethoxy)benzoyl]-N-(2-methylpropyl)-, methyl ester
    2. Synonyms:
    3. CAS NO:681465-96-3
    4. Molecular Formula: C20H29NO4
    5. Molecular Weight: 347.455
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 681465-96-3.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: L-Alanine, N-[4-ethenyl-3-(1-methylethoxy)benzoyl]-N-(2-methylpropyl)-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: L-Alanine, N-[4-ethenyl-3-(1-methylethoxy)benzoyl]-N-(2-methylpropyl)-, methyl ester(681465-96-3)
    11. EPA Substance Registry System: L-Alanine, N-[4-ethenyl-3-(1-methylethoxy)benzoyl]-N-(2-methylpropyl)-, methyl ester(681465-96-3)
  • 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: 681465-96-3(Hazardous Substances Data)

681465-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 681465-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,1,4,6 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 681465-96:
(8*6)+(7*8)+(6*1)+(5*4)+(4*6)+(3*5)+(2*9)+(1*6)=193
193 % 10 = 3
So 681465-96-3 is a valid CAS Registry Number.

681465-96-3Relevant articles and documents

Terephthalamide peptidomimetic compounds and methods

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Page/Page column 2; sheet 3, (2010/11/27)

The present invention relates to compounds and pharmaceutical compositions based upon terephthalamide which are proteomimetic and to methods for inhibiting the interaction of an alpha-helical protein with another protein or binding site. Methods for treat

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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