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2,4-Dibromo-6-fluorobenzoic acid, with the molecular formula C7H3Br2FO2, is a white to off-white solid chemical compound. It is recognized for its potent herbicidal properties, making it a valuable component in agricultural and land management practices for controlling a broad spectrum of broadleaf weeds.

183065-69-2

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183065-69-2 Usage

Uses

Used in Agricultural Industry:
2,4-DIBROMO-6-FLUOROBENZOIC ACID is used as a pesticide and herbicide for its ability to effectively control a wide range of broadleaf weeds in various crop and non-crop land management systems. It functions by disrupting the growth and reproduction processes of targeted weeds, ultimately resulting in their death.
Used in Environmental Management:
2,4-DIBROMO-6-FLUOROBENZOIC ACID is used as a tool in environmental management to maintain the health and productivity of land areas by preventing the overgrowth of unwanted vegetation, thus preserving the intended use of the land and minimizing the need for manual or mechanical weed control methods.

Check Digit Verification of cas no

The CAS Registry Mumber 183065-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,0,6 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 183065-69:
(8*1)+(7*8)+(6*3)+(5*0)+(4*6)+(3*5)+(2*6)+(1*9)=142
142 % 10 = 2
So 183065-69-2 is a valid CAS Registry Number.

183065-69-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Dibromo-6-fluorobenzoic acid

1.2 Other means of identification

Product number -
Other names PC0739

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:183065-69-2 SDS

183065-69-2Relevant academic research and scientific papers

INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL

-

Page/Page column 93, (2010/11/18)

This invention relates to compounds having structural Formula I: and pharmaceutically acceptable salts thereof which are inhibitors of the Renal Outer Medullary Potassium (ROMK) channel (Kir1.1). The compounds of Formula I are useful as diuretics and natriuretics and therefore are useful for the therapy and prophylaxis of disorders resulting from excessive salt and water retention, including cardiovascular diseases such as hypertension and chronic and acute heart failure

INHIBITORS OF STEAROYL-COA DESATURASE

-

, (2009/06/27)

Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of diseases such as, for example, obesity.

Substitution effect on the regioselective halogen/metal exchange of 3-substituted 1,2,5-tribromobenzenes

Menzel, Karsten,Mills, Paul M.,Frantz, Doug E.,Nelson, Todd D.,Kress, Michael H.

, p. 415 - 418 (2008/09/17)

Regioselective halogen/metal exchange reactions using isopropylmagnesium chloride were studied on 3-substituted 1,2,5-tribromoarenes. Seven examples are given.

Dihydroquinazolinones as 5HT modulators

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Page/Page column 19-20, (2008/06/13)

The present application provides modulators of serotonin receptors, pharmaceutical compositions containing such modulators and methods for treating various diseases, conditions and disorders associated with modulation of serotonin receptors such as, for e

Regioselective ortho-lithiation of chloro and bromo substituted fluoroarenes

Mongin, Florence,Schlosser, Manfred

, p. 6551 - 6554 (2007/10/03)

Deprotonation of fluoroarenes carrying chlorine or bromine as additional substituents occurs always at a fluorine adjacent position if accomplished with potassium tert-butoxide activated butyllithium or lithium 2,2,6,6-tetramethylpiperidide.

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