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4-methyl-N-<2-(4-methyl-2-quinolinyl)phenyl>-2-quinolinamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127727-05-3 Structure
  • Basic information

    1. Product Name: 4-methyl-N-<2-(4-methyl-2-quinolinyl)phenyl>-2-quinolinamine
    2. Synonyms:
    3. CAS NO:127727-05-3
    4. Molecular Formula:
    5. Molecular Weight: 375.473
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127727-05-3.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: 4-methyl-N-<2-(4-methyl-2-quinolinyl)phenyl>-2-quinolinamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-methyl-N-<2-(4-methyl-2-quinolinyl)phenyl>-2-quinolinamine(127727-05-3)
    11. EPA Substance Registry System: 4-methyl-N-<2-(4-methyl-2-quinolinyl)phenyl>-2-quinolinamine(127727-05-3)
  • 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: 127727-05-3(Hazardous Substances Data)

127727-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127727-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,7,2 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 127727-05:
(8*1)+(7*2)+(6*7)+(5*7)+(4*2)+(3*7)+(2*0)+(1*5)=133
133 % 10 = 3
So 127727-05-3 is a valid CAS Registry Number.

127727-05-3Downstream Products

127727-05-3Relevant articles and documents

Reinvestigation of a 5H-Dibenzotriazonine Synthesis

Peet, Norton P.,Sunder, Shyam,Barbuch, Robert J.,Whalon, Michael R.,Huber, Edward W.,Huffman, John C.

, p. 1611 - 1618 (2007/10/02)

Treatment of 5-chloro-2-aminobenzophenone (1) with o-phenylenediamine, sodium acetate, and acetic acid gave 2-(acetyl)amino-5-chlorobenzophenone (5) rather than N--1,2-benzenediamine (3), as reported by Kulkarni et al.Authentic 3 was prepared and treated with chloroacetic acid and polyphosphoric acid (PPA) to give 1, recovered 3, 2,8-dichloro-6,12-diphenyldibenzodiazocine (9) and 2-chloro-6-(chloromethyl)-13-phenyl-5H-dibenzotriazonine (10).Treatment of 5 with PPA, with or without chloroacetic acid, gave phenyl> phenylmethanone (11) as the sole product in 90percent yield.Treatment of other benzophenones, acetophenones, and anilines with sodium acetate and acetic acid provided acetanilides in 78-96percent yield, with the exception of 2'-aminoacetophenone (20), wich gave a quantitative yield of 2--4-methylquinoline (21).The mechanism of acetanilide formation with sodium acetate and acetic acid is discussed.The structure of 21 was established using high resolution 1H nmr techniques.Attempts to prepare an authentic sample of 21 from 2-chlorolepidine (26) and (20) gave 4-methyl-N--2-quinolinamine (29) as the major product.

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