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4-Amino-8-fluoroquinoline, a quinoline derivative with the molecular formula C9H7FN2, is a chemical compound that features an amino group and a fluorine atom. It is recognized for its antiparasitic and antibacterial properties, which make it a significant building block in the synthesis of pharmaceuticals, particularly antimalarial drugs. Its molecular structure and reactivity contribute to its versatility in medicinal chemistry and drug discovery.

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  • 148401-38-1 Structure
  • Basic information

    1. Product Name: 4-AMINO-8-FLUOROQUINOLINE
    2. Synonyms: IFLAB-BB F2108-0096;BUTTPARK 100\09-76;4-AMINO-8-FLUOROQUINOLINE;4-Quinolinamine,8-fluoro-(9CI);8-fluoro-4-quinolinamine(SALTDATA: FREE);8-Fluoroquinolin-4-aMine
    3. CAS NO:148401-38-1
    4. Molecular Formula: C9H7FN2
    5. Molecular Weight: 162.16
    6. EINECS: N/A
    7. Product Categories: HALIDE
    8. Mol File: 148401-38-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 335.8°C at 760 mmHg
    3. Flash Point: 156.9°C
    4. Appearance: /
    5. Density: 1.315g/cm3
    6. Vapor Pressure: 0.000117mmHg at 25°C
    7. Refractive Index: 1.676
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 5.96±0.50(Predicted)
    11. CAS DataBase Reference: 4-AMINO-8-FLUOROQUINOLINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-AMINO-8-FLUOROQUINOLINE(148401-38-1)
    13. EPA Substance Registry System: 4-AMINO-8-FLUOROQUINOLINE(148401-38-1)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22-41
    3. Safety Statements: 26-39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 148401-38-1(Hazardous Substances Data)

148401-38-1 Usage

Uses

Used in Pharmaceutical Industry:
4-Amino-8-fluoroquinoline is used as a key intermediate in the synthesis of various pharmaceuticals, primarily for the development of antimalarial drugs. Its antiparasitic properties are instrumental in creating effective treatments against malaria-causing parasites.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-Amino-8-fluoroquinoline serves as a versatile chemical building block, facilitating the design and synthesis of new medications with potential applications in treating a range of diseases, including bacterial infections.
Used in Drug Discovery:
4-Amino-8-fluoroquinoline is utilized in drug discovery processes to explore its potential in creating novel compounds with enhanced therapeutic effects. Its unique molecular structure allows for modifications that can improve drug efficacy, selectivity, and safety profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 148401-38-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,4,0 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 148401-38:
(8*1)+(7*4)+(6*8)+(5*4)+(4*0)+(3*1)+(2*3)+(1*8)=121
121 % 10 = 1
So 148401-38-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H7FN2/c10-7-3-1-2-6-8(11)4-5-12-9(6)7/h1-5H,(H2,11,12)

148401-38-1SDS

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 8-fluoroquinolin-4-amine

1.2 Other means of identification

Product number -
Other names 4-Amino-8-fluoroquinoline

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:148401-38-1 SDS

148401-38-1Upstream product

148401-38-1Relevant articles and documents

N-(4-pyridyl or 4-quinolinyl) arylacetamide and 4-(aralkoxy or aralkylamino) pyridine pesticides

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, (2008/06/13)

N-(4-Pyridyl or 4-quinolinyl) arylacetamides, for example N-((3-chloro-2-ethyl)-4-pyridyl)(4-(4-chlorophenoxy) phenyl)-acetamide, and 4-(aralkyoxy or aralkylamino)pyridines, for example 4-[2-[4-(2,2,2-trifluoroethoxy)phenyl]ethoxy]pyridine, are active aga

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