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2-(N,N-Dimethylaminosulfonyl)phenylboronic acid pinacol ester, also known as DMAPB pinacol, is a boronic acid derivative that is widely used in organic synthesis as a reagent for Suzuki-Miyaura cross-coupling reactions. It is a versatile compound known for its ability to effectively and selectively functionalize a variety of substrates. DMAPB pinacol ester is valued for its stability, low toxicity, and high efficiency in organic reactions, making it a preferred choice in research and industrial settings.

486422-06-4

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486422-06-4 Usage

Uses

Used in Pharmaceutical Synthesis:
2-(N,N-Dimethylaminosulfonyl)phenylboronic acid pinacol ester is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to selectively functionalize substrates, contributing to the development of new and improved drugs.
Used in Agricultural Chemical Production:
In the agricultural industry, 2-(N,N-Dimethylaminosulfonyl)phenylboronic acid pinacol ester serves as a crucial component in the production of agricultural chemicals, enhancing the efficiency and selectivity of chemical reactions required for creating effective and targeted agrochemicals.
Used in Advanced Material Development:
2-(N,N-Dimethylaminosulfonyl)phenylboronic acid pinacol ester is utilized as a reagent in the development of advanced materials, where its unique properties allow for the creation of materials with specific functionalities and improved performance characteristics.
Used in Cancer Research and Treatment:
2-(N,N-Dimethylaminosulfonyl)phenylboronic acid pinacol ester is investigated for its potential in the treatment of cancer and other diseases, leveraging its reactivity in organic synthesis to develop compounds that can target and treat specific types of cancer.
Used in Organic Synthesis Research:
In research settings, 2-(N,N-Dimethylaminosulfonyl)phenylboronic acid pinacol ester is employed as a reagent for Suzuki-Miyaura cross-coupling reactions, facilitating the study and development of new synthetic pathways and methodologies in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 486422-06-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,6,4,2 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 486422-06:
(8*4)+(7*8)+(6*6)+(5*4)+(4*2)+(3*2)+(2*0)+(1*6)=164
164 % 10 = 4
So 486422-06-4 is a valid CAS Registry Number.

486422-06-4SDS

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 2-(N,N-Dimethylsulfamoyl)phenylboronic acid. pinacol ester

1.2 Other means of identification

Product number -
Other names N,N-dimethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

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:486422-06-4 SDS

486422-06-4Upstream product

486422-06-4Downstream Products

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