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3-(Methylsulfonyl)phenylboronic Acid Pinacol Ester is a boronic acid ester derivative that is widely used in organic synthesis and drug discovery. It features a boron atom attached to a phenyl ring with a pinacol group, which contributes to its unique reactivity and selectivity in forming carbon-carbon bonds. This chemical compound is a valuable tool in organic chemistry research and drug development due to its versatility and efficiency in creating complex molecular structures.

1001185-88-1

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  • 2-(3-methanesulfonylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

    Cas No: 1001185-88-1

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1001185-88-1 Usage

Uses

Used in Organic Synthesis:
3-(Methylsulfonyl)phenylboronic Acid Pinacol Ester is used as a building block in organic synthesis for its ability to efficiently form carbon-carbon bonds in complex molecules. Its reactivity and selectivity make it a preferred choice for constructing various organic compounds.
Used in Drug Discovery:
In the pharmaceutical industry, 3-(Methylsulfonyl)phenylboronic Acid Pinacol Ester is used as a key intermediate in the synthesis of biologically active compounds and potential drug candidates. Its ability to selectively form carbon-carbon bonds allows for the creation of diverse and complex molecular structures with potential therapeutic applications.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
3-(Methylsulfonyl)phenylboronic Acid Pinacol Ester is used as a reagent in Suzuki-Miyaura cross-coupling reactions, a fundamental method for forming carbon-carbon bonds in organic chemistry. This reaction is widely employed in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and materials.
Overall, 3-(Methylsulfonyl)phenylboronic Acid Pinacol Ester is a versatile and valuable compound in the fields of organic synthesis, drug discovery, and chemical research, owing to its unique properties and applications in forming carbon-carbon bonds in complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 1001185-88-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,1,1,8 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1001185-88:
(9*1)+(8*0)+(7*0)+(6*1)+(5*1)+(4*8)+(3*5)+(2*8)+(1*8)=91
91 % 10 = 1
So 1001185-88-1 is a valid CAS Registry Number.

1001185-88-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4,5,5-tetramethyl-2-(3-methylsulfonylphenyl)-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names Z-4517

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:1001185-88-1 SDS

1001185-88-1Downstream Products

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