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4-(N-Thiomorpholinylsulfonyl)phenylboronic Acid is a chemical compound that belongs to the class of organoboronic acids and esters. It is also an organosulfur compound, known for its role as a reagent in various chemical reactions, particularly the Suzuki-Miyaura cross-coupling reactions. 4-(N-THIOMORPHOLINYLSULFONYL)PHENYLBORONIC ACID is composed of Boron, Carbon, Hydrogen, Nitrogen, Oxygen, and Sulfur, and is typically found in solid form. Its utility is highly valued in scientific research, especially in the field of synthetic chemistry. As with other chemicals in its class, adherence to safety and handling instructions is crucial when working with 4-(N-Thiomorpholinylsulfonyl)phenylboronic Acid.

871329-69-0

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871329-69-0 Usage

Uses

Used in Synthetic Chemistry:
4-(N-Thiomorpholinylsulfonyl)phenylboronic Acid is used as a reagent in synthetic chemistry for facilitating Suzuki-Miyaura cross-coupling reactions. This reaction is a widely used method for the formation of carbon-carbon bonds, particularly in the synthesis of complex organic molecules and pharmaceutical compounds.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 4-(N-Thiomorpholinylsulfonyl)phenylboronic Acid is utilized as a key intermediate in the synthesis of various drug molecules. Its ability to participate in cross-coupling reactions allows for the creation of diverse molecular structures with potential therapeutic applications.
Used in Research and Development:
4-(N-Thiomorpholinylsulfonyl)phenylboronic Acid is employed in research and development settings to explore new chemical reactions and synthetic pathways. Its unique properties and reactivity make it a valuable tool for advancing the understanding of chemical processes and discovering novel compounds with potential applications in various fields.
Used in Material Science:
In material science, 4-(N-Thiomorpholinylsulfonyl)phenylboronic Acid may be used as a component in the development of new materials with specific properties. Its involvement in cross-coupling reactions can contribute to the creation of materials with tailored characteristics for use in various applications, such as electronics, coatings, or advanced materials for specific industries.

Check Digit Verification of cas no

The CAS Registry Mumber 871329-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,3,2 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 871329-69:
(8*8)+(7*7)+(6*1)+(5*3)+(4*2)+(3*9)+(2*6)+(1*9)=190
190 % 10 = 0
So 871329-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H14BNO4S2/c13-11(14)9-1-3-10(4-2-9)18(15,16)12-5-7-17-8-6-12/h1-4,13-14H,5-8H2

871329-69-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H52907)  4-(4-Thiomorpholinylsulfonyl)benzeneboronic acid, 98%   

  • 871329-69-0

  • 250mg

  • 1296.0CNY

  • Detail

871329-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-(Thiomorpholinosulfonyl)phenyl)boronic acid

1.2 Other means of identification

Product number -
Other names (4-thiomorpholin-4-ylsulfonylphenyl)boronic acid

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:871329-69-0 SDS

871329-69-0Upstream product

871329-69-0Relevant academic research and scientific papers

New phenylpyridylpiperazine compounds

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Page/Page column 7, (2008/06/13)

A compound selected from those of formula (I): [image] wherein: X represents a C(O) or SO2 group, R1 represents an aryl group or a group NR3R4 wherein R3 and R4 are as defined in the description, R2 represents an alkyl, (C3-C8)cycloalkyl or (C3-C8)cycloalkyl-(C1-C6)alkyl group, its isomers, and addition salts thereof, and medicinal products containing the same which are useful in treating conditions treatable by antagonists of type H3 central histamine receptors.

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