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2-Chloro-7-Methoxyquinoline, a member of the quinoline family, is a chemical compound characterized by the molecular formula C10H7ClNO. It features a chloro and methoxy group at specific positions on the quinoline ring, which endows it with unique chemical and biological properties. This versatile compound has garnered interest in various scientific and industrial fields due to its potential applications.

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  • 49609-15-6 Structure
  • Basic information

    1. Product Name: 2-Chloro-7-Methoxyquinoline
    2. Synonyms: 2-Chloro-7-Methoxyquinoline;QUINOLINE, 2-CHLORO-7-METHOXY-
    3. CAS NO:49609-15-6
    4. Molecular Formula: C10H8ClNO
    5. Molecular Weight: 193.62962
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 49609-15-6.mol
  • Chemical Properties

    1. Melting Point: 97-98 °C
    2. Boiling Point: 145 °C(Press: 0.6 Torr)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.267±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. PKA: 0.65±0.50(Predicted)
    10. CAS DataBase Reference: 2-Chloro-7-Methoxyquinoline(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Chloro-7-Methoxyquinoline(49609-15-6)
    12. EPA Substance Registry System: 2-Chloro-7-Methoxyquinoline(49609-15-6)
  • 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: 49609-15-6(Hazardous Substances Data)

49609-15-6 Usage

Uses

Used in Pharmaceutical Synthesis:
2-Chloro-7-Methoxyquinoline is utilized as a precursor in the synthesis of pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic benefits. 2-Chloro-7-Methoxyquinoline's reactivity and functional groups make it a valuable building block in medicinal chemistry.
Used in Agrochemical Production:
In the agrochemical industry, 2-Chloro-7-Methoxyquinoline serves as a key intermediate in the production of various agrochemicals. Its incorporation into these products can enhance their effectiveness in controlling pests and diseases, thereby contributing to improved crop yields and food security.
Used in Antimicrobial Research:
2-Chloro-7-Methoxyquinoline has been studied for its antimicrobial properties, making it a potential candidate for the development of new antimicrobial agents. Its ability to inhibit the growth of various microorganisms could lead to the creation of novel treatments for infectious diseases.
Used in Anticancer Research:
2-Chloro-7-Methoxyquinoline has also been investigated for its anticancer properties, with research exploring its potential to target and inhibit the growth of cancer cells. As a result, 2-Chloro-7-Methoxyquinoline may contribute to the development of innovative cancer therapies, offering new hope for patients and healthcare professionals.

Check Digit Verification of cas no

The CAS Registry Mumber 49609-15-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,0 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 49609-15:
(7*4)+(6*9)+(5*6)+(4*0)+(3*9)+(2*1)+(1*5)=146
146 % 10 = 6
So 49609-15-6 is a valid CAS Registry Number.

49609-15-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-7-methoxyquinoline

1.2 Other means of identification

Product number -
Other names Quinoline,2-chloro-7-methoxy

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:49609-15-6 SDS

49609-15-6Relevant articles and documents

BICYCLIC ETHER O-GLYCOPROTEIN-2-ACETAMIDO-2-DEOXY-3-D-GLUCOPYRANOSIDASE INHIBITORS

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Paragraph 00195, (2020/08/22)

Described herein are compounds represented by formula (I) or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising the same and methods of preparing and using the same. The variables Ar, X, R1, R3, R 4, Y1, Y2, n and p are as defined herein.

NOVEL 6-6 BICYCLIC AROMATIC RING SUBSTITUTED NUCLEOSIDE ANALOGUES FOR USE AS PRMT5 INHIBITORS

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, (2017/03/14)

The present invention relates novel 6-6 bicyclic aromatic ring substituted nucleoside analogues of Formula (I) wherein the variables have the meaning defined in the claims. The compounds according to the present invention are useful as PRMT5 inhibitors. The invention further relates to pharmaceutical compositions comprising said compounds as an active ingredient as well as the use of said compounds as a medicament.

BIARYLTRIAZOLE INHIBITORS OF MACROPHAGE MIGRATION INHIBITORY FACTOR

-

, (2016/09/22)

The present disclosure describes biaryl triazole compounds, as well as their compositions and methods of use. The compounds inhibit the activity of macrophage migration inhibitory factor and are useful for the treatment of diseases, e.g., inflammatory dis

TRIAZOLO-PYRAZINE DERIVATIVES USEFUL IN THE TREATMENT OF DISORDERS OF THE CENTRAL NERVOUS SYSTEM

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Paragraph 00222, (2014/06/23)

Provided herein are heteroaryl compounds, methods of their synthesis, pharmaceutical compositions comprising the compounds, and methods of their use. In one embodiment, the compounds provided herein are useful for the treatment, prevention, and/or management of various disorders, such as CNS disorders and metabolic disorders, including, but not limited to, e.g., neurological disorders, psychosis, schizophrenia, obesity, and diabetes.

II. Synthesis and biological evaluation of some bioisosteres and congeners of the antitumor agent, 2-{4-[(7-chloro-2-quinoxalinyl)oxylphenoxy}propionic acid (XK469)

Hazeldine, Stuart T.,Polin, Lisa,Kushner, Juiwanna,White, Kathryn,Bouregeois, Nicole M.,Crantz, Brianna,Palomino, Eduardo,Corbett, Thomas H.,Horwitz, Jerome P.

, p. 3130 - 3137 (2007/10/03)

XK469 (1) is among the most highly and broadly active antitumor agents to have been evaluated in our laboratories. Subsequent developmental studies led to the entry of (R)-(+) 1 (NSC 698215) into phase 1 clinical trials (NIH UO1-CA62487). The antitumor me

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