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CAS

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19701-33-8

3-Methyl-quinolin-4-ylamine, a chemical compound with the molecular formula C10H10N2, belongs to the quinoline class of compounds. It is a versatile building block in the pharmaceutical industry, used for the synthesis of various drug molecules. 3-METHYL-QUINOLIN-4-YLAMINE possesses potential medicinal properties, making it a significant interest to both the pharmaceutical and chemical industries.

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  • 19701-33-8 Structure

  • Basic information

    1. Product Name: 3-METHYL-QUINOLIN-4-YLAMINE
    2. Synonyms: 4-AMINO-3-METHYLQUINOLINE;3-METHYL-QUINOLIN-4-YLAMINE;4-Quinolinamine,3-methyl-(9CI);3-Methyl-4-quinolinamine
    3. CAS NO:19701-33-8
    4. Molecular Formula: C10H10N2
    5. Molecular Weight: 158.1998
    6. EINECS: N/A
    7. Product Categories: ISOQUINOLINE;API intermediates
    8. Mol File: 19701-33-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 340.6°Cat760mmHg
    3. Flash Point: 186.5°C
    4. Appearance: /
    5. Density: 1.169g/cm3
    6. Vapor Pressure: 8.49E-05mmHg at 25°C
    7. Refractive Index: 1.681
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-METHYL-QUINOLIN-4-YLAMINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-METHYL-QUINOLIN-4-YLAMINE(19701-33-8)
    12. EPA Substance Registry System: 3-METHYL-QUINOLIN-4-YLAMINE(19701-33-8)

  • 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: 19701-33-8(Hazardous Substances Data)

19701-33-8 Usage

Uses

Used in Pharmaceutical Industry:
3-Methyl-quinolin-4-ylamine is used as a key intermediate in the synthesis of pharmaceuticals for its potential applications in developing anti-inflammatory, antimicrobial, and anticancer drugs. Its versatile nature allows for the creation of a wide range of medicinal compounds.
Used in Research and Development:
In the field of research and development, 3-methyl-quinolin-4-ylamine serves as a valuable compound for studying its potential medicinal properties and exploring new avenues for drug discovery and innovation. Its presence in various drug synthesis pathways makes it an essential component in advancing pharmaceutical science.

Check Digit Verification of cas no

The CAS Registry Mumber 19701-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,0 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19701-33:
(7*1)+(6*9)+(5*7)+(4*0)+(3*1)+(2*3)+(1*3)=108
108 % 10 = 8
So 19701-33-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2/c1-7-6-12-9-5-3-2-4-8(9)10(7)11/h2-6H,1H3,(H2,11,12)

19701-33-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylquinolin-4-amine

1.2 Other means of identification

Product number -
Other names 4-amino-3-methylquinoline

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:19701-33-8 SDS

19701-33-8Downstream Products

19701-33-8Relevant articles and documents

Symmetrical bis-quinolinium compounds: New human choline kinase inhibitors with antiproliferative activity against the HT-29 cell line

Sánchez-Martín, Rosario,Campos, Joaquín M.,Conejo-García, Ana,Cruz-López, Olga,Bá?ez-Coronel, Mónica,Rodríguez-González, Agustín,Gallo, Miguel A.,Lacal, Juan C.,Espinosa, Antonio

, p. 3354 - 3363 (2007/10/03)

Studies have been aimed at the establishment of structure-activity relationships that define choline kinase inhibitory and antiproliferative activities of 40 bisquinolinium compounds. These derivatives have electron-releasing groups at position 4 of the q

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