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5-Amino-3-benzyl-3H-imidazole-4-carboxylic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 169616-29-9 Structure
  • Basic information

    1. Product Name: 5-Amino-3-benzyl-3H-imidazole-4-carboxylic acid ethyl ester
    2. Synonyms: 5-Amino-3-benzyl-3H-imidazole-4-carboxylic acid ethyl ester;4-Amino-1-benzyl-1H-imidazole-5-carboxylic acid ethyl ester
    3. CAS NO:169616-29-9
    4. Molecular Formula: C13H15N3O2
    5. Molecular Weight: 245
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 169616-29-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 443.9±30.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.22
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 4.76±0.61(Predicted)
    10. CAS DataBase Reference: 5-Amino-3-benzyl-3H-imidazole-4-carboxylic acid ethyl ester(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-Amino-3-benzyl-3H-imidazole-4-carboxylic acid ethyl ester(169616-29-9)
    12. EPA Substance Registry System: 5-Amino-3-benzyl-3H-imidazole-4-carboxylic acid ethyl ester(169616-29-9)
  • 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: 169616-29-9(Hazardous Substances Data)

169616-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169616-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,6,1 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 169616-29:
(8*1)+(7*6)+(6*9)+(5*6)+(4*1)+(3*6)+(2*2)+(1*9)=169
169 % 10 = 9
So 169616-29-9 is a valid CAS Registry Number.

169616-29-9Relevant articles and documents

Imidazopyrazinones (IPYs): Non-Quinolone Bacterial Topoisomerase Inhibitors Showing Partial Cross-Resistance with Quinolones

Jeannot, Frédéric,Taillier, Thomas,Despeyroux, Pierre,Renard, Stéphane,Rey, Astrid,Mourez, Micha?l,Poeverlein, Christoph,Khichane, Imène,Perrin, Marc-Antoine,Versluys, Stéphanie,Stavenger, Robert A.,Huang, Jianzhong,Germe, Thomas,Maxwell, Anthony,Cao, Sha,Huseby, Douglas L.,Hughes, Diarmaid,Bacqué, Eric

, p. 3565 - 3581 (2018)

In our quest for new antibiotics able to address the growing threat of multidrug resistant infections caused by Gram-negative bacteria, we have investigated an unprecedented series of non-quinolone bacterial topoisomerase inhibitors from the Sanofi patrim

Discovery, synthesis and biochemical profiling of purine-2,6-dione derivatives as inhibitors of the human poly(A)-selective ribonuclease Caf1

Jadhav, Gopal P.,Kaur, Ishwinder,Maryati, Maryati,Airhihen, Blessing,Fischer, Peter M.,Winkler, G. Sebastiaan

, p. 4219 - 4224 (2015)

Eukaryotic mRNA contains a 3′ poly(A) tail, which plays important roles in the regulation of mRNA stability and translation. Well-characterized enzymes involved in the shortening of the poly(A) tail include the multi-subunit Ccr4-Not deadenylase, which contains the Caf1 (Pop2) and Ccr4 catalytic components, and poly(A)-specific ribonuclease (PARN). Two Mg2+ ions present in the active sites of these ribonucleases are required for RNA cleavage. Here, we report the discovery, synthesis and biochemical profiling of purine-2,6-dione derivatives as (sub)micromolar inhibitors of Caf1.

1-Substituted xanthines

Bridson,Wang

, p. 855 - 858 (2007/10/02)

A convenient general procedure for the preparation of 1-alkyl-, 1-aryl-, and 1-aminoxanthines from an easily prepared imidazole precursor is described.

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