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CAS

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356761-10-9

4-(benzyloxy)-2-(chloroMethyl)-3-Methylquinoline is a quinoline derivative with the molecular formula C21H18ClNO. It is an aromatic compound that features a quinoline ring with a benzyloxy group, a chloromethyl group, and a methyl group attached to it. This chemical compound is utilized in organic synthesis and medicinal chemistry as a building block for the preparation of various pharmaceutical compounds. Its molecular structure indicates potential biological activities and therapeutic applications.

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  • 356761-10-9 Structure

  • Basic information

    1. Product Name: 4-(benzyloxy)-2-(chloroMethyl)-3-Methylquinoline
    2. Synonyms: 4-(benzyloxy)-2-(chloroMethyl)-3-Methylquinoline
    3. CAS NO:356761-10-9
    4. Molecular Formula: C18H16ClNO
    5. Molecular Weight: 297.77874
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 356761-10-9.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: 4-(benzyloxy)-2-(chloroMethyl)-3-Methylquinoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(benzyloxy)-2-(chloroMethyl)-3-Methylquinoline(356761-10-9)
    11. EPA Substance Registry System: 4-(benzyloxy)-2-(chloroMethyl)-3-Methylquinoline(356761-10-9)

  • 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: 356761-10-9(Hazardous Substances Data)

356761-10-9 Usage

Uses

Used in Pharmaceutical Industry:
4-(benzyloxy)-2-(chloroMethyl)-3-Methylquinoline is used as a key intermediate in the synthesis of pharmaceutical compounds for its potential biological activities and therapeutic applications. Its unique molecular structure allows it to be a valuable building block in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(benzyloxy)-2-(chloroMethyl)-3-Methylquinoline is used as a precursor in the production of agrochemicals. Its chemical properties make it suitable for the synthesis of compounds that can be used in pest control and crop protection.
Used in Organic Synthesis:
4-(benzyloxy)-2-(chloroMethyl)-3-Methylquinoline is utilized as a versatile building block in organic synthesis. Its functional groups enable it to participate in various chemical reactions, making it a valuable component in the creation of complex organic molecules for research and commercial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 356761-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,6,7,6 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 356761-10:
(8*3)+(7*5)+(6*6)+(5*7)+(4*6)+(3*1)+(2*1)+(1*0)=159
159 % 10 = 9
So 356761-10-9 is a valid CAS Registry Number.

356761-10-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(chloromethyl)-3-methyl-4-phenylmethoxyquinoline

1.2 Other means of identification

Product number -
Other names 4-Benzyloxy-2-chloromethyl-3-methyl-quinoline

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:356761-10-9 SDS

356761-10-9Relevant articles and documents

Profiling structural diversity and activity of 2-alkyl-4(1H)-quinoloneN-oxides ofPseudomonasandBurkholderia

B?ttcher, Thomas,Dieterich, Cora Lisbeth,Prothiwa, Michaela,Szamosvári, Dávid

, p. 6328 - 6331 (2020/06/21)

We synthesized all major saturated and unsaturated 2-alkyl-4(1H)-quinoloneN-oxides ofPseudomonasandBurkholderia, quantified their native production levels and characterized their antibiotic activities against competingStaphylococcus aureus. We demonstrate that quinolone core methylation and position of unsaturation in the alkyl-chain dictate antibiotic potency which supports the proposed mechanism of action.

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