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2-FLUORO-3-METHOXYBENZOYL CHLORIDE is a chemical compound with the molecular formula C8H6ClFO2. It is a benzoic acid derivative with a fluorine atom and a methoxy group attached to the benzene ring. 2-FLUORO-3-METHOXYBENZOYL CHLORIDE is classified as a chloroformyl chloride, meaning it contains a carbon atom bonded to a chlorine atom and a carbonyl group.

850563-45-0

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850563-45-0 Usage

Uses

Used in Organic Synthesis:
2-FLUORO-3-METHOXYBENZOYL CHLORIDE is used as a reagent for the introduction of the benzoic acid functionality into various organic molecules. It aids in the formation of new compounds with potential applications in various fields.
Used in Pharmaceutical Industry:
2-FLUORO-3-METHOXYBENZOYL CHLORIDE is used as an intermediate in the pharmaceutical industry for the production of various drugs. Its unique structure allows for the development of new medicinal compounds with specific therapeutic properties.
Used in Agrochemical Industry:
2-FLUORO-3-METHOXYBENZOYL CHLORIDE is also utilized as an intermediate in the agrochemical industry for the production of pesticides. Its incorporation into these products can enhance their effectiveness in controlling pests and diseases in agriculture.
Used in Research and Industrial Applications:
2-FLUORO-3-METHOXYBENZOYL CHLORIDE is a key building block for the development of novel materials and compounds for research and industrial applications. Its versatility in chemical reactions makes it a valuable component in creating innovative products and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 850563-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,5,6 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 850563-45:
(8*8)+(7*5)+(6*0)+(5*5)+(4*6)+(3*3)+(2*4)+(1*5)=170
170 % 10 = 0
So 850563-45-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClFO2/c1-12-6-4-2-3-5(7(6)10)8(9)11/h2-4H,1H3

850563-45-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-FLUORO-3-METHOXYBENZOYL CHLORIDE

1.2 Other means of identification

Product number -
Other names 2-fluoranyl-3-methoxy-benzoyl chloride

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:850563-45-0 SDS

850563-45-0Relevant academic research and scientific papers

Site-Selective Silylation of Aliphatic C-H Bonds Mediated by [1,5]-Hydrogen Transfer: Synthesis of α-Sila Benzamides

Liu, Pei,Tang, Jinghua,Zeng, Xiaoming

supporting information, p. 5536 - 5539 (2016/11/17)

The first example of site-selective silylation of C(sp3)-H bonds mediated by a [1,5]-hydrogen transfer is reported. This reaction occurs selectively at the α-position of benzamides with a combination of tert-butylmagnesium chloride and a catalytic amount of 4,4′-di-tert-butylbipyridine (dtbpy) ligand and provides a facile route for the creation of biologically interesting α-sila benzamides. Late-stage functionalization of the incorporated silyl moieties facilitates the synthesis of N-formyl, cis-enamine, β-hydroxyl, amino, and pyrrole-containing derivatives.

Antibacterial alkoxybenzamide inhibitors of the essential bacterial cell division protein FtsZ

Czaplewski, Lloyd G.,Collins, Ian,Boyd, E. Andrew,Brown, David,East, Stephen P.,Gardiner, Mihaly,Fletcher, Rowena,Haydon, David J.,Henstock, Vincent,Ingram, Peter,Jones, Clare,Noula, Caterina,Kennison, Leanne,Rockley, Chris,Rose, Valerie,Thomaides-Brears, Helena B.,Ure, Rebecca,Whittaker, Mark,Stokes, Neil R.

scheme or table, p. 524 - 527 (2011/02/28)

3-Methoxybenzamide is a weak inhibitor of the essential bacterial cell division protein FtsZ. Exploration of the structure-activity relationships of 3-methoxybenzamide analogues led to the identification of potent anti-staphylococcal compounds.

HETEROARYL COMPOUNDS, COMPOSITIONS THEREOF, AND USE THEREOF AS PROTEIN KINASE INHIBITORS

-

Page/Page column 181, (2008/12/05)

Provided herein are Heteroaryl Compounds having the following structure: (I) wherein R1, R2, L, X, Y, Z, Q, A and B are as defined herein, compositions comprising an effective amount of a Heteroaryl Compound and methods for treating or preventing cancer, inflammatory conditions, immunological conditions, metabolic conditions and conditions treatable or preventable by inhibition of a kinase pathway comprising administering an effective amount of a Heteroaryl Compound to a patient in need thereof.

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