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6-Quinolinecarboxamide,N,N-dimethyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 847248-48-0 Structure
  • Basic information

    1. Product Name: 6-Quinolinecarboxamide,N,N-dimethyl-(9CI)
    2. Synonyms: 6-Quinolinecarboxamide,N,N-dimethyl-(9CI)
    3. CAS NO:847248-48-0
    4. Molecular Formula: C12H12N2O
    5. Molecular Weight: 200.23648
    6. EINECS: N/A
    7. Product Categories: PYRIDINE
    8. Mol File: 847248-48-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-Quinolinecarboxamide,N,N-dimethyl-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-Quinolinecarboxamide,N,N-dimethyl-(9CI)(847248-48-0)
    11. EPA Substance Registry System: 6-Quinolinecarboxamide,N,N-dimethyl-(9CI)(847248-48-0)
  • 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: 847248-48-0(Hazardous Substances Data)

847248-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 847248-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,2,4 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 847248-48:
(8*8)+(7*4)+(6*7)+(5*2)+(4*4)+(3*8)+(2*4)+(1*8)=200
200 % 10 = 0
So 847248-48-0 is a valid CAS Registry Number.

847248-48-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-Dimethyl-6-quinolinecarboxamide

1.2 Other means of identification

Product number -
Other names Benzenamine,N,N,4-trimethyl-,hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:847248-48-0 SDS

847248-48-0Downstream Products

847248-48-0Relevant articles and documents

Preparation method of quinoline amide compounds

-

Paragraph 0027-0028, (2020/12/10)

The invention belongs to the technical field of organic synthesis, and particularly discloses a preparation method of quinoline amide compounds, which comprises the following steps: (1) adding quinoline carboxylic acid compounds and thiuram into an organic solvent to react to obtain a reaction solution; and (2) separating and purifying the reaction solution obtained in the step (1). According to the invention, a one-pot boiling method is adopted, an economical and easily available quinoline carboxylic acid compound and thiuram are used as raw materials, and an amidation reaction is directly carried out in air to generate the corresponding quinoline amide compound. The synthesis system is wide in application range, compatible with functional groups such as quinolyl and acylamino, simple inprocess, convenient to operate, mild in reaction condition, wide in substrate range, high in yield and suitable for application and popularization.

Design of novel nicotinic ligands through 3D database searching

Guandalini, Luca,Martini, Elisabetta,Dei, Silvia,Manetti, Dina,Scapecchi, Serena,Teodori, Elisabetta,Romanelli, M. Novella,Varani, Katia,Greco, Giovanni,Spadola, Loredana,Novellino, Ettore

, p. 799 - 807 (2007/10/03)

A series of quinoline derivatives have been designed on the basis of results from a 3D search of the Cambridge Structural Database using the nicotinic pharmacophore as a query and further modified using molecular modeling. Some of the synthesized compound

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