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3-Bromo-5-(difluoromethyl)pyridine, 97% is a pyridine derivative with the molecular formula C6H4BrF2N. It features a bromine atom and two fluorine atoms attached to the carbon ring, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Available in a high purity grade of 97%, this chemical is suitable for research and industrial applications and is recognized for its potential as a reagent in the production of complex organic molecules.

114468-04-1

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114468-04-1 Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-5-(difluoromethyl)pyridine, 97% is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with improved therapeutic properties and reduced side effects.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Bromo-5-(difluoromethyl)pyridine, 97% serves as a crucial building block for the creation of novel pesticides and herbicides. Its incorporation into these products can enhance their effectiveness and selectivity, leading to better crop protection and reduced environmental impact.
Used in Advanced Materials:
3-Bromo-5-(difluoromethyl)pyridine, 97% is utilized as a precursor in the development of advanced materials with unique properties. These materials can be employed in various applications, such as electronics, energy storage, and nanotechnology, where their specific characteristics provide advantages over traditional materials.
Used in Research Applications:
As a high-purity chemical compound, 3-Bromo-5-(difluoromethyl)pyridine, 97% is an essential tool for researchers in academia and industry. It enables the exploration of new chemical reactions, the synthesis of novel compounds, and the investigation of structure-property relationships in various fields of chemistry and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 114468-04-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,4,6 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 114468-04:
(8*1)+(7*1)+(6*4)+(5*4)+(4*6)+(3*8)+(2*0)+(1*4)=111
111 % 10 = 1
So 114468-04-1 is a valid CAS Registry Number.

114468-04-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H34371)  3-Bromo-5-(difluoromethyl)pyridine, 97%   

  • 114468-04-1

  • 250mg

  • 582.0CNY

  • Detail
  • Alfa Aesar

  • (H34371)  3-Bromo-5-(difluoromethyl)pyridine, 97%   

  • 114468-04-1

  • 1g

  • 1688.0CNY

  • Detail
  • Aldrich

  • (741329)  3-Bromo-5-(difluoromethyl)pyridine  97%

  • 114468-04-1

  • 741329-500MG

  • 1,064.70CNY

  • Detail

114468-04-1SDS

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 3-Bromo-5-(difluoromethyl)pyridine

1.2 Other means of identification

Product number -
Other names -

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:114468-04-1 SDS

114468-04-1Downstream Products

114468-04-1Relevant articles and documents

FLUOROALKYL-OXADIAZOLES AND USES THEREOF

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Paragraph 00362-00363, (2021/06/26)

Provided herein are compounds identified as inhibitors of HDAC6 activity that can be used to treat various diseases and disorders.

ALDOSTERONE SYNTHASE INHIBITORS

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Page/Page column 35, (2016/12/26)

The present invention relates to compounds of formula I: and pharmaceutically acceptable salts thereof, wherein R1, R2 and R3, are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.

5-SUBSTITUTED INDAZOLE-3-CARBOXAMIDES AND PREPARATION AND USE THEREOF

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Paragraph 1274; 1275, (2015/11/09)

Indazole compounds for treating various diseases and pathologies are disclosed. More particularly, the present disclosure concerns the use of an indazole compound or analogs thereof, in the treatment of disorders characterized by the activation of Wnt pathway signaling (e.g., cancer, abnormal cellular proliferation, angiogenesis, Alzheimer's disease, lung disease, fibrotic disorders, cartilage (chondral) defects, and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, and neurological conditions/disorders/diseases linked to overexpression of DYRK1A.

Compounds and their use as BACE Inhibitors

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Page/Page column 40, (2012/07/13)

The present invention relates to compounds of formula (I) and their pharmaceutical compositions. In addition, the present invention relates to therapeutic methods for the treatment and/or prevention of Aβ-related pathologies such as Down's syndrome, β-amyloid angiopathy such as but not limited to cerebral amyloid angiopathy or hereditary cerebral hemorrhage, disorders associated with cognitive impairment such as but not limited to MCI (“mild cognitive impairment”), Alzheimer's disease, memory loss, attention deficit symptoms associated with Alzheimer's disease, neurodegeneration associated with diseases such as Alzheimer's disease or dementia including dementia of mixed vascular and degenerative origin, pre-senile dementia, senile dementia and dementia associated with Parkinson's disease, progressive supranuclear palsy or cortical basal degeneration.

Syntheses of New Aromatic Compounds with Fluorinated Side Chains and their Chemical Reactivity

Haas, Alois,Spitzer, Martin,Lieb, Max

, p. 1329 - 1340 (2007/10/02)

The syntheses of a wide range of aromatic compounds of the type p-Y-C6H4CF2X(4-13) are described, and the chemical behavior of these compounds as a function of substituent Y is investigated .Analogously the pyridine derivatives 15, 17, and 18 were synthesized and characterized.From a correlation of the 19F-NMR data of these compounds with the Hammett constant of Y, participation of C-F ?-back-donation is seen as the cause for an observed shift of the 19F signals to lower field.

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