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3-Bromo-4-chloro-5-fluoropyridine is a pyridine derivative with the molecular formula C5H2BrClFN. It belongs to the aromatic heterocyclic compounds, featuring a ring of five carbon atoms and one nitrogen atom. 3-broMo-4-chloro-5-fluoropyridine is distinguished by the presence of bromine, chlorine, and fluorine atoms attached to the 3rd, 4th, and 5th carbon atoms, respectively. Its unique structure and the presence of halogen atoms make it a valuable intermediate and building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals, facilitating a broad spectrum of chemical transformations and applications.

1211540-92-9

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1211540-92-9 Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-4-chloro-5-fluoropyridine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its versatile structure allows for the introduction of different functional groups, enabling the development of new drugs with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 3-bromo-4-chloro-5-fluoropyridine serves as a building block for the creation of novel agrochemicals. Its unique halogenated structure contributes to the development of effective pesticides, herbicides, and other crop protection agents.
Used in Fine Chemicals Synthesis:
3-Bromo-4-chloro-5-fluoropyridine is utilized as a versatile starting material in the synthesis of fine chemicals. Its ability to undergo various chemical transformations makes it suitable for the production of specialty chemicals, dyes, and other high-value compounds.
Used in Chemical Research:
This pyridine derivative is also employed as a research tool in chemical laboratories. Its unique structure and reactivity make it an interesting subject for studying reaction mechanisms, exploring new synthetic routes, and developing innovative applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1211540-92-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,1,5,4 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1211540-92:
(9*1)+(8*2)+(7*1)+(6*1)+(5*5)+(4*4)+(3*0)+(2*9)+(1*2)=99
99 % 10 = 9
So 1211540-92-9 is a valid CAS Registry Number.

1211540-92-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-4-chloro-5-fluoropyridine

1.2 Other means of identification

Product number -
Other names 3-BROMO-4-CHLORO-5-FLUOROPYRIDINE

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:1211540-92-9 SDS

1211540-92-9Relevant academic research and scientific papers

BIARYL DERIVATIVE AND MEDICINE CONTAINING SAME

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Paragraph 0282; 0283, (2018/08/07)

Provided is a compound showing excellent antifungal activity against Trichophyton fungus, which is a major causative microorganism of superficial mycosis, and high effectiveness on diseases caused by Trichophyton fungi. A biaryl derivative represented by the formula (I) or a salt thereof: wherein ring A is an optionally substituted phenyl, or an optionally substituted 5- or 6-membered ring heteroaryl (ring A may be further condensed to form an optionally substituted fused ring); Q is CH2, C=O, NH, O, S or the like; X1, X2 and X3 are CR1 or N; Y is CH or N; Z is CR2b or N; R2a and R2b are each a hydrogen atom, a halogen atom, an optionally substituted C1-C6 alkyl group, a C1-C6 haloalkyl group or the like; R2a and R2b may form, together with carbon atoms bonded thereto, an optionally substituted carbocycle, or an optionally substituted heterocycle.

PHARMACEUTICALS COMPRISING BIARYL DERIVATIVES OR SALTS THEREOF

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Paragraph 0283; 0284; 0285, (2018/10/24)

PROBLEM TO BE SOLVED: To provide compounds with excellent antimycotic activity against Trichophyton. SOLUTION: The invention provides pharmaceuticals comprising biaryl derivatives represented by general formula (I) or salts thereof, where ring A is optionally substituted phenyl or the like; Q is CH2 or the like; X1, X2 and X3 are CR1 or the like; and Y is CH or N. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

COMPOUNDS USEFUL AS INHIBITORS OF ATR KINASE

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Paragraph 0503; 0505, (2015/06/17)

The present invention relates to compounds useful as inhibitors of ATR protein kinase. The invention relates to pharmaceutically acceptable compositions comprising the compounds of this invention; methods of treating of various diseases, disorders, and conditions using the compounds of this invention; processes for preparing the compounds of this invention; intermediates for the preparation of the compounds of this invention; and solid forms of the compounds of this invention. The compounds of this invention have formula I-A or I-B: wherein the variables are as defined herein.

COMPOUNDS USEFUL AS INHIBITORS OF ATR KINASE

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Paragraph 00243, (2015/06/18)

The present invention relates to compounds useful as inhibitors of ATR protein kinase. The invention also relates to pharmaceutically acceptable compositions comprising the compounds of this invention; methods of treating of various diseases, disorders, a

COMPOUNDS USEFUL AS INHIBITORS OF ATR KINASE

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Paragraph 0309; 0310, (2015/06/17)

The present invention relates to compounds useful as inhibitors of ATR protein kinase. The invention also relates to pharmaceutically acceptable compositions comprising the compounds of this invention; methods of treating of various diseases, disorders, a

COMPOUNDS USEFUL AS INHIBITORS OF ATR KINASE

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Paragraph 00371; 00372, (2014/06/24)

The present invention relates to compounds useful as inhibitors of ATR protein kinase. The invention also relates to pharmaceutically acceptable compositions comprising the compounds of this invention; methods of treating of various diseases, disorders, and conditions using the compounds of this invention; processes for preparing the compounds of this invention; intermediates for the preparation of the compounds of this invention; and methods of using the compounds in in vitro applications, such as the study of kinases in biological and pathological phenomena; the study of intracellular signal transduction pathways mediated by such kinases; and the comparative evaluation of new kinase inhibitors. The compounds of this invention have formula (I) or a pharmaceutically acceptable salt, wherein the variables are as devined herein. Moreover, The compounds of this invention have formula (I-A) or a pharmaceutically acceptable salt, wherein the variables are as defined herein.

FUSED PYRAZOLOPYRIMIDINE DERIVATIVES USEFUL AS INHIBITORS OF ATR KINASE

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Paragraph 00260-00261, (2014/09/29)

The present invention relates to compounds useful as inhibitors of ATR protein kinase. The invention also relates to pharmaceutically acceptable compositions comprising the compounds of this invention; methods of treating of various diseases, disorders, a

COMPOUNDS USEFUL AS INHIBITORS OF ATR KINASE

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Paragraph 00263-00264, (2014/09/29)

The present invention relates to compounds useful as inhibitors of ATR protein kinase. The invention also relates to pharmaceutically acceptable compositions comprising the compounds of this invention; methods of treating of various diseases, disorders, and conditions using the compounds of this invention; processes for preparing the compounds of this invention; intermediates for the preparation of the compounds of this invention; and methods of using the compounds in in vitro applications, such as the study of kinases in biological and pathological phenomena; the study of intracellular signal transduction pathways mediated by such kinases; and the comparative evaluation of new kinase inhibitors. The compounds of this invention have formula (I); or a pharmaceutically acceptable salt, wherein the variables R1, R2, R3, and R4 are as defined herein.

ALDOSTERONE SYNTHASE INHIBITORS

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Page/Page column 54, (2012/11/13)

This invention relates to tricyclic triazole analogues of the formula I or their pharmaceutically acceptable salts, wherein the variable are defined herein. The inventive compounds selectively inhibit aldosterone synthetase. This invention also provides for pharmaceutical compositions comprising the compounds of Formula I or their salts as well as to methods for the treatment, amelioration or prevention of conditions that could be treated by inhibiting aldosterone synthetase.

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