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7-chloro-4-phenoxyquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124495-03-0 Structure
  • Basic information

    1. Product Name: 7-chloro-4-phenoxyquinoline
    2. Synonyms: 7-chloro-4-phenoxyquinoline
    3. CAS NO:124495-03-0
    4. Molecular Formula:
    5. Molecular Weight: 255.703
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124495-03-0.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: 7-chloro-4-phenoxyquinoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-chloro-4-phenoxyquinoline(124495-03-0)
    11. EPA Substance Registry System: 7-chloro-4-phenoxyquinoline(124495-03-0)
  • 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: 124495-03-0(Hazardous Substances Data)

124495-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124495-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,9 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 124495-03:
(8*1)+(7*2)+(6*4)+(5*4)+(4*9)+(3*5)+(2*0)+(1*3)=120
120 % 10 = 0
So 124495-03-0 is a valid CAS Registry Number.

124495-03-0Downstream Products

124495-03-0Relevant articles and documents

Lewis acid-catalyzed generation of C-C and C-N bonds on π-deficient heterocyclic substrates

Staderini, Matteo,Bolognesi, Maria Laura,Menndez, J. Carlos

, p. 185 - 195 (2015)

Focused microwave irradiation of a series of halogenated nitrogen heterocycles and different kinds of nucleophiles in the presence of a catalytic amount of indium trichloride leads to the efficient and completely regioselective generation of aromatic C-C and C-N bonds. The method is simple, rapid, general and inexpensive, and can be performed without the use of dried solvents. Most of the synthetized compounds are new and in many cases the work-up required only filtration. Furthermore, this is the first example of the use of a Lewis acid as a catalyst for heteroarylation, vinylation and amination reactions on π-deficient heterocyclic substrates.

A new class of artificial nucleases that recognize and cleave apurinic sites in DNA with great selectivity and efficiency

Fkyerat, Abdellatif,Demeunynck, Martine,Constant, Jean-Fran?ois,Michon, Pierre,Lhomme, Jean

, p. 9952 - 9959 (1993)

A series of tailor-made molecules, 1 and 4-7, have been prepared to recognize and cleave DNA at apurinic sites. These molecules incorporate in their structure different units designed for specific functions: (1) an intercalator for DNA binding, (2) a nucl

SYNTHESIS OF N-ACRIDINYL AND N-QUINOLINYL DERIVATIVES OF RADIOPROTECTIVE AMINO-THIOLS

Demonchaux, Patrice,Laayoun, Ali,Demeunynck, Martine,Lhomme, Jean

, p. 6455 - 6466 (2007/10/02)

A series of bifunctional molecules in which a heterocycle is linked to an aminothiol chain were synthesized.A new synthesis of N,N'-bis-(3-aminopropyl) cystamine (WR 33278) is descrided.Reaction of WR 33278 or analogues with the phenoxy derivatives of qui

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