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3,5-bis(difluoromethyl)-1H-pyrazole(SALTDATA: FREE), also known as a pyrazole derivative, is a chemical compound characterized by the presence of two difluoromethyl groups. It is recognized for its diverse applications across various industries, including pharmaceuticals, agrochemicals, and materials science, due to its unique chemical properties and potential for synthesis into a wide array of products.

77614-79-0

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77614-79-0 Usage

Uses

Used in Pharmaceutical Industry:
3,5-bis(difluoromethyl)-1H-pyrazole(SALTDATA: FREE) is used as a building block for the synthesis of various pharmaceuticals, leveraging its chemical structure to create new drugs with potential therapeutic benefits.
Used in Agrochemical Industry:
In the agrochemical sector, 3,5-bis(difluoromethyl)-1H-pyrazole(SALTDATA: FREE) is utilized as a component in the development of agrochemicals, such as pesticides and fungicides, due to its antimicrobial and antifungal properties, which contribute to crop protection and yield enhancement.
Used in Materials Science:
3,5-bis(difluoromethyl)-1H-pyrazole(SALTDATA: FREE) is employed in materials science for the development of novel polymers and additives, taking advantage of its chemical properties to improve material performance and create innovative products with specific applications.
Used in Research Applications:
3,5-bis(difluoromethyl)-1H-pyrazole(SALTDATA: FREE) serves as a valuable compound in research settings, where its diverse biological activities, such as antimicrobial, antifungal, and pesticidal properties, are explored for potential new discoveries and applications in various scientific fields.

Check Digit Verification of cas no

The CAS Registry Mumber 77614-79-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,1 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77614-79:
(7*7)+(6*7)+(5*6)+(4*1)+(3*4)+(2*7)+(1*9)=160
160 % 10 = 0
So 77614-79-0 is a valid CAS Registry Number.

77614-79-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-Bis(difluoromethyl)-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 3,5-bis(difluoromethyl)pyrazole

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:77614-79-0 SDS

77614-79-0Relevant academic research and scientific papers

A Major Advance in the Synthesis of Fluoroalkyl Pyrazoles: Tuneable Regioselectivity and Broad Substitution Patterns

Schmitt, Etienne,Panossian, Armen,Vors, Jean-Pierre,Funke, Christian,Lui, Norbert,Pazenok, Sergiy,Leroux, Frédéric R.

, p. 11239 - 11244 (2016/08/03)

A novel approach towards highly functionalized fluoroalkyl pyrazoles was developed by using fluoroalkyl amino reagents in combination with a variety of fluorinated ketimines. Tuneable introduction of fluoroalkyl groups in the 3- and 5-positions was possible by using vinamidinium intermediates or the corresponding enamino ketones after hydrolysis. These high-value building blocks can give rise to a large number of analogues for bioactivity screening and discovering new heterocyclic bioactive ingredients in various life science fields.

Method for the production of 3,5-bis(fluoroalkyl) pyrazole derivatives

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Paragraph 0176; 0177; 0178; 0179; 0180; 0181, (2016/10/10)

The invention relates to a method for producing 3,5-bis(fluoroalkyl) pyrazole derivatives and to the use thereof for producing fungicides. Also claimed are intermediates of formulae (IV) and (III).

METHOD FOR THE PRODUCTION OF 3,5-BIS(FLUOROALKYL)PYRAZOLE DERIVATIVES

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Paragraph 0148; 0149; 0150; 0151, (2016/06/01)

The present invention describes a novel method for preparing 3,5-bis(fluoroalkyl)pyrazole derivatives.

PROCESS FOR PREPARING 3,5-BIS(HALOALKYL)PYRAZOLE DERIVATIVES VIA ACYLATION OF HYDRAZONES

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Page/Page column 13, (2016/01/01)

Process for preparing 3,5-bis(haloalkyl)pyrazole derivatives of the formula (I), via acylation of Hydrazones.

PROCESS FOR PREPARING 3,5-BIS(HALOALKYL)PYRAZOLES VIA ACYLATION OF KETIMINES

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Page/Page column 12, (2016/01/01)

The present invention relates to a novel process for preparing 3,5-bis(haloalkyl)pyrazole derivatives of the formula (Ia) and (Ib), via acylation of ketimines.

PROCESS FOR PREPARING 3,5-BIS(HALOALKYL)PYRAZOLE DERIVATIVES FROM α,α-DIHALOAMINES AND KETIMINES

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Page/Page column 19-20, (2015/11/24)

Process for preparine3,5-bis(haloalkyl)pyrazolederivatives from a,a-dihaloamines and ketimines The present invention relates to a novel process for preparing 3,5-bis(haloalkyl)pyrazole derivatives from a,a-dihaloamines and ketimines. Intermedaites used in the process are also claimed.

A General Approach towards NH-Pyrazoles That Bear Diverse Fluoroalkyl Groups by Means of Fluorinated Iminium Salts

Schmitt, Etienne,Landelle, Grégory,Vors, Jean-Pierre,Lui, Norbert,Pazenok, Sergiy,Leroux, Frédéric R.

supporting information, p. 6052 - 6060 (2015/09/22)

A new and general approach to important fluoroalkyl-substituted pyrazoles has been developed. The approach is based on the use of fluoroalkyl amino reagents and their Lewis acid activation to form a fluoroalkyl iminium salt that acts as a formal "fluoroacyl transfer reagent". Their interaction with readily available fluoroalkyl azines followed by spontaneous cyclization of the formed intermediates under acidic conditions leads to the formation of 3,5-disubstituted pyrazoles. The reaction is extremely versatile, high yielding, and allows quick access to pyrazoles that bear two fluoroalkyl functionalities (identical or different). These compounds are otherwise difficult to prepare. The reaction is scalable and suitable for industrial production.

PROCESS FOR PREPARING 3,5-BIS(HALOALKYL)PYRAZOLE DERIVATIVES FROM α,α-DIHALOAMINES

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Page/Page column 15, (2015/05/26)

The present invention relates to a novel process for preparing 3,5-bis(haloalkyl)pyrazole derivatives.

PROCESS FOR PREPARING 3,5-BIS(FLUOROALKYL)PYRAZOLE DERIVATIVES FROM α,α-DIHALOAMINES

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Page/Page column 15-16, (2014/12/12)

The present invention relates to a novel process for preparing 3,5-bis(fluoroalkyl)pyrazole derivatives from α,α-dihaloamines.

PROCESS FOR THE PREPARATION OF BIS-DIHALOALKYL PYRAZOLES

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, (2014/09/03)

The present invention relates to a process for the preparation of bisdihaloalkyl pyrazoles of formula (V) starting from diketones and acylhalides reacted with a Lewis acid, and a subsequent reaction with a substituted hydrazine.

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