Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2,4-Diisobutyl-quinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

123005-16-3 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 123005-16-3 Structure
  • Basic information

    1. Product Name: 2,4-Diisobutyl-quinoline
    2. Synonyms: 2,4-Diisobutyl-quinoline
    3. CAS NO:123005-16-3
    4. Molecular Formula:
    5. Molecular Weight: 241.376
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123005-16-3.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: 2,4-Diisobutyl-quinoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-Diisobutyl-quinoline(123005-16-3)
    11. EPA Substance Registry System: 2,4-Diisobutyl-quinoline(123005-16-3)
  • 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: 123005-16-3(Hazardous Substances Data)

123005-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123005-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,0,0 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 123005-16:
(8*1)+(7*2)+(6*3)+(5*0)+(4*0)+(3*5)+(2*1)+(1*6)=63
63 % 10 = 3
So 123005-16-3 is a valid CAS Registry Number.

123005-16-3Downstream Products

123005-16-3Relevant articles and documents

Homolytic alkylation of heteroaromatic bases : The problem of monoalkylation

Fontana,Minisci,Barbosa, M. C. Nogueira,Vismara

, p. 2525 - 2538 (1990)

The silver-catalyzed decarboxylation of carboxylic acids by persulphate leads to alkyl radicals, which have been utilized for the selective alkylation of heteroaromatic bases. The method is particularly efficient in a water-chlorobenzene two-phase system for two reasons : it considerably increases the selectivity in monoalkylation when more positions of high nucleophilic reactivity (i.e. α and γ) are available in the heterocyclic ring (i.e. quinoline , 4-cyano- and 4-ethylpyridine, pyrazine , quinoxaline etc.) and it determines a much higher efficiency for the radical sources when the silver salt catalysis is deactivated by complexation of the salt with the heterocyclic compound . The high selectivity in monoalkylation has been obtained by the combination of polar effects and the increased lipophilicity of the alkylated product, which makes its extraction from the aqueous solution by the organic solvent easier.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 123005-16-3