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1-(Benzenesulfonyl)-1H-pyrazole-4-boronic acid pinacol ester is a chemical compound characterized by a pyrazole ring, a boronic acid pinacol ester group, and a benzenesulfonyl substituent. It is recognized for its versatile reactivity and the presence of functional groups that are significant in the synthesis of biologically active molecules and pharmaceuticals.

1073372-04-9

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  • 1-(Phenylsulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

    Cas No: 1073372-04-9

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  • SAGECHEM/1-(Phenylsulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole/SAGECHEM/Manufacturer in China

    Cas No: 1073372-04-9

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1073372-04-9 Usage

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Used in Organic Synthesis:
1-(Benzenesulfonyl)-1H-pyrazole-4-boronic acid pinacol ester is used as a building block for the creation of complex organic compounds, particularly those with biological activity. Its unique structure allows for the formation of a wide range of molecules that can be further utilized in various applications.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 1-(Benzenesulfonyl)-1H-pyrazole-4-boronic acid pinacol ester is used as a key intermediate in the synthesis of drugs. Its presence of boronic acid and sulfonyl groups makes it a valuable component in the development of new medications with potential therapeutic benefits.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
1-(Benzenesulfonyl)-1H-pyrazole-4-boronic acid pinacol ester is utilized as a reagent in Suzuki-Miyaura cross-coupling reactions. This reaction is a widely used method in organic chemistry for the formation of carbon-carbon bonds, which is essential in the synthesis of complex organic compounds, including those with potential applications in materials science and medicinal chemistry.
Used in Materials Science:
In materials science, 1-(Benzenesulfonyl)-1H-pyrazole-4-boronic acid pinacol ester is used for the development of new materials with specific properties. 1-(Benzenesulfonyl)-1H-pyrazole-4-boronic acid pinacol ester's reactivity and functional groups contribute to the creation of materials with unique characteristics that can be applied in various technological and industrial fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1073372-04-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,3,7 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1073372-04:
(9*1)+(8*0)+(7*7)+(6*3)+(5*3)+(4*7)+(3*2)+(2*0)+(1*4)=129
129 % 10 = 9
So 1073372-04-9 is a valid CAS Registry Number.
InChI:InChI=1S/C15H19BN2O4S/c1-14(2)15(3,4)22-16(21-14)12-10-17-18(11-12)23(19,20)13-8-6-5-7-9-13/h5-11H,1-4H3

1073372-04-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H26954)  1-Phenylsulfonyl-1H-pyrazole-4-boronic acid pinacol ester, 95%   

  • 1073372-04-9

  • 250mg

  • 1117.0CNY

  • Detail
  • Alfa Aesar

  • (H26954)  1-Phenylsulfonyl-1H-pyrazole-4-boronic acid pinacol ester, 95%   

  • 1073372-04-9

  • 1g

  • 2577.0CNY

  • Detail

1073372-04-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Phenylsulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 1-(benzenesulfonyl)-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:1073372-04-9 SDS

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