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2-Chloro-8-fluoroquinoline, a quinoline derivative with the molecular formula C9H5ClFN, is a chemical compound that features both chlorine and fluorine substituents. It is known for its antimicrobial and antiparasitic properties, which render it valuable for pharmaceutical and medicinal applications. Additionally, its structural and reactive characteristics make it a versatile building block for the synthesis of various organic compounds, and it may serve as a starting material for the development of new drugs. However, due to its potential hazards, it is crucial to handle and use 2-Chloro-8-fluoroquinoline with caution.

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  • 124467-23-8 Structure
  • Basic information

    1. Product Name: 2-Chloro-8-fluoroquinoline
    2. Synonyms: 2-Chloro-8-fluoroquinoline
    3. CAS NO:124467-23-8
    4. Molecular Formula: C9H5ClFN
    5. Molecular Weight: 181.5941032
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124467-23-8.mol
  • Chemical Properties

    1. Melting Point: 82-84℃
    2. Boiling Point: 271.3±20.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.366±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Room temperature.
    8. Solubility: N/A
    9. PKA: -2.73±0.50(Predicted)
    10. CAS DataBase Reference: 2-Chloro-8-fluoroquinoline(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Chloro-8-fluoroquinoline(124467-23-8)
    12. EPA Substance Registry System: 2-Chloro-8-fluoroquinoline(124467-23-8)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22-41
    3. Safety Statements: 26-39
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 124467-23-8(Hazardous Substances Data)

124467-23-8 Usage

Uses

Used in Pharmaceutical and Medicinal Applications:
2-Chloro-8-fluoroquinoline is used as an active pharmaceutical ingredient for its antimicrobial and antiparasitic properties, contributing to the development of treatments for various infections and parasitic diseases.
Used in Agrochemical Production:
2-Chloro-8-fluoroquinoline is utilized as a key intermediate in the synthesis of agrochemicals, playing a role in the development of pesticides and other agricultural products to protect crops and enhance yields.
Used in Specialty Chemicals:
2-Chloro-8-fluoroquinoline is employed as a building block in the production of specialty chemicals, where its unique structure and reactivity are leveraged to create novel compounds for specific industrial applications.
Used in Organic Synthesis:
As a versatile starting material, 2-Chloro-8-fluoroquinoline is used in organic synthesis for the preparation of a wide range of organic compounds, including potential drug candidates and other chemical entities with specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 124467-23-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,6 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 124467-23:
(8*1)+(7*2)+(6*4)+(5*4)+(4*6)+(3*7)+(2*2)+(1*3)=118
118 % 10 = 8
So 124467-23-8 is a valid CAS Registry Number.

124467-23-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H33446)  2-Chloro-8-fluoroquinoline, 95%   

  • 124467-23-8

  • 250mg

  • 671.0CNY

  • Detail
  • Alfa Aesar

  • (H33446)  2-Chloro-8-fluoroquinoline, 95%   

  • 124467-23-8

  • 1g

  • 1862.0CNY

  • Detail
  • Aldrich

  • (759988)  2-Chloro-8-fluoroquinoline  95%

  • 124467-23-8

  • 759988-1G

  • 1,170.00CNY

  • Detail

124467-23-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-8-fluoroquinoline

1.2 Other means of identification

Product number -
Other names Quinoline,2-chloro-8-fluoro

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:124467-23-8 SDS

124467-23-8Relevant articles and documents

HETEROCYCLIC COMPOUNDS AND THEIR USES

-

, (2013/10/22)

Substituted bicyclic heteroaryls and compositions containing them, for the treatment of general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, including but not restricted to autoimmune diseases such as systemic lupus erythematosis (SLE), myestenia gravis, rheumatoid arthritis, acute disseminated encephalomyelitis, idiopathic thrombocytopenic purpura, multiples sclerosis, Sjoegren's syndrome and autoimmune hemolytic anemia, allergic conditions including all forms of hypersensitivity, The present invention also enables methods for treating cancers that are mediated, dependent on or associated with p110δ activity, including but not restricted to leukemias, such as Acute Myeloid leukaemia (AML) Myelo-dysplastic syndrome (MDS) myelo-proliferative diseases (MPD) Chronic Myeloid Leukemia (CML) T-cell Acute Lymphoblastic leukaemia (T-ALL) B-cell Acute Lymphoblastic leukaemia (B-ALL) Non Hodgkins Lymphoma (NHL) B-cell lymphoma and solid tumors, such as breast cancer.

TRIAZOLOPYRIDINE COMPOUNDS AS PIM KINASE INHIBITORS

-

Page/Page column 116, (2010/04/03)

Compounds of Formula (I), in which A, B, R1, R1a, R2, R3, R4, R5, R6, and R7 have the meanings given in the specification, are receptor tyrosine inhibitors useful in the treatment of immune cell-associated diseases and disorders, such as inflammatory and autoimmune diseases.

HETEROCYCLIC COMPOUNDS AND THEIR USES

-

, (2008/12/04)

Substituted bicyclic heteroaryls and compositions containing them, for the treatment of general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, including but not restricted to autoimmune diseases such as systemic lupus erythematosis (SLE), myestenia gravis, rheumatoid arthritis, acute disseminated encephalomyelitis, idiopathic thrombocytopenic purpura, multiples sclerosis, Sjoegren's syndrome and autoimmune hemolytic anemia, allergic conditions including all forms of hypersensitivity. The present invention also enables methods for treating cancers that are mediated, dependent on, or associated with p110 activity, including but not restricted to leukemias, such as acute myeloid leukaemia (AML), myelo-dysplastic syndrome (MDS), myelo-proliferative diseases (MPD), chronic myeloid leukemia (CML), T-cell acute lymphoblastic leukaemia (T-ALL), B-cell acute lymphoblastic leukaemia (B-ALL), non Hodgkins lymphoma (NHL), B-cell lymphoma and solid tumors, such as breast cancer.

Elemental fluorine Part 15. Selective direct fluorination of quinoline derivatives

Chambers, Richard D.,Holling, Darren,Sandford, Graham,Batsanov, Andrei S.,Howard, Judith A.K.

, p. 661 - 671 (2007/10/03)

Direct fluorination of various quinoline derivatives in acidic reaction media gives fluorinated quinoline products arising from electrophilic substitution processes.

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