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3,5-Dimethyl-1-(tetrahydro-2H-pyran-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol95% is a pyrazole derivative chemical compound with a purity of 95%. It features a tetrahydro-2H-pyran-2-yl and a dioxaborolan-2-yl group, making it a versatile building block in various chemical applications.

1126779-11-0

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1126779-11-0 Usage

Uses

Used in Organic Synthesis:
3,5-Dimethyl-1-(tetrahydro-2H-pyran-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol95% is used as a key intermediate in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. Its unique structure allows for the creation of complex organic molecules through various chemical reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3,5-Dimethyl-1-(tetrahydro-2H-pyran-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol95% is used as a building block for the development of new drugs. Its pyrazole core and functional groups enable the design of bioactive molecules with potential therapeutic properties.
Used in Agrochemical Industry:
3,5-Dimethyl-1-(tetrahydro-2H-pyran-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol95% is also utilized in the agrochemical industry as a precursor for the synthesis of novel agrochemicals. Its structural features can be exploited to create compounds with pesticidal or herbicidal properties.
Used in Materials Science:
In materials science, 3,5-Dimethyl-1-(tetrahydro-2H-pyran-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol95% has potential applications in the development of new materials with unique properties. Its chemical structure can be incorporated into polymers, coatings, or other materials to enhance their performance.
Used as a Ligand in Organometallic Chemistry:
3,5-Dimethyl-1-(tetrahydro-2H-pyran-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol95% can be employed as a ligand in organometallic chemistry. Its ability to coordinate with metal centers can lead to the development of new catalysts for various chemical transformations, improving reaction efficiency and selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 1126779-11-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,6,7,7 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1126779-11:
(9*1)+(8*1)+(7*2)+(6*6)+(5*7)+(4*7)+(3*9)+(2*1)+(1*1)=160
160 % 10 = 0
So 1126779-11-0 is a valid CAS Registry Number.

1126779-11-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H32478)  3,5-Dimethyl-1-(2-tetrahydropyranyl)-1H-pyrazole-4-boronic acid pinacol ester, 95%   

  • 1126779-11-0

  • 250mg

  • 1264.0CNY

  • Detail
  • Alfa Aesar

  • (H32478)  3,5-Dimethyl-1-(2-tetrahydropyranyl)-1H-pyrazole-4-boronic acid pinacol ester, 95%   

  • 1126779-11-0

  • 1g

  • 3499.0CNY

  • Detail

1126779-11-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(THP)-3,5-Dimethylpyrazole-4-boronic acid, pinacol ester

1.2 Other means of identification

Product number -
Other names 3,5-dimethyl-1-(oxan-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)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:1126779-11-0 SDS

1126779-11-0Relevant academic research and scientific papers

SUBSTITUTED PYRAZOLE DERIVATIVES

-

Page/Page column 33-34, (2009/10/31)

The present invention provides a novel pyrazole derivative and an androgen receptor antagonist containing the derivative. The present invention provides a compound represented by the formula (I′) wherein R1 is a hydrogen atom, a group via a carbon atom, a group via a nitrogen atom, a group via an oxygen atom, or a group via a sulfur atom; R2 is a phenyl group having cyano (the phenyl group may further have substituent(s) other than cyano); R3 is a hydrogen atom, a group via a carbon atom, a group via a nitrogen atom, a group via an oxygen atom, or a group via a sulfur atom; R4 is a cyclic group optionally having substituent(s); and X is methylene optionally having substituent(s), or CO, or a salt thereof.

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