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2,3-Dihydrobenzofuran-5-boronic acid pinacol ester is a specialty chemical compound characterized by its benzofuran ring structure, which is a fusion of benzene and furan rings. As a boronic ester, it features a pinacol moiety, a type of diol with two hydroxyl groups attached to the same carbon atom, which is crucial for the ester formation. 2,3-Dihydrobenzofuran-5-boronic acid pinacol ester is widely recognized for its utility in organic chemistry, particularly in the field of pharmaceutical and agrochemical development.

937591-69-0

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937591-69-0 Usage

Uses

Used in Organic Chemistry Research:
2,3-Dihydrobenzofuran-5-boronic acid pinacol ester is used as a reagent in organic chemistry for its unique properties that facilitate Suzuki coupling reactions. These reactions are palladium-catalyzed cross-coupling processes that enable the formation of carbon-carbon bonds, which are fundamental in constructing complex organic molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2,3-Dihydrobenzofuran-5-boronic acid pinacol ester is utilized as a key intermediate in the synthesis of various drug molecules. Its ability to participate in Suzuki coupling reactions allows for the creation of diverse molecular structures with potential therapeutic applications.
Used in Agrochemical Development:
Similarly, in agrochemicals, 2,3-Dihydrobenzofuran-5-boronic acid pinacol ester serves as a vital building block for the synthesis of compounds with pesticidal or herbicidal properties. Its role in forming carbon-carbon bonds through Suzuki coupling is essential for the development of new and effective agrochemicals.
Overall, 2,3-Dihydrobenzofuran-5-boronic acid pinacol ester is a versatile and indispensable compound in the realms of scientific research and chemical synthesis, particularly for the advancement of pharmaceuticals and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 937591-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,7,5,9 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 937591-69:
(8*9)+(7*3)+(6*7)+(5*5)+(4*9)+(3*1)+(2*6)+(1*9)=220
220 % 10 = 0
So 937591-69-0 is a valid CAS Registry Number.

937591-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 2-(2,3-dihydro-1-benzofuran-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

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:937591-69-0 SDS

937591-69-0Downstream Products

937591-69-0Relevant academic research and scientific papers

MLL1 INHIBITORS AND ANTI-CANCER AGENTS

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Page/Page column 33-34, (2021/04/01)

The present invention provides a compound of Formula (I): or an enantiomer, an enantiomeric mixture, or a pharmaceutically acceptable salt thereof; wherein the variables are as defined herein. The present invention further provides pharmaceutical compositions comprising such compounds; and methods of using such compounds for treating a disease or condition mediated by mixed lineage leukemia 1 (MLL).

PYRIMIDINE SULFAMIDE DERIVATIVE AND PREPARATION METHOD AND MEDICAL APPLICATION THEREOF

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Paragraph 0327; 0330-0331, (2020/09/22)

Disclosed are a series of pyrimidine sulfamide compounds and applications thereof in preparing a drug for a disease related to an ETA receptor antagonist. In particular, disclosed is a derived compound represented by formula (I) or a tautomer or pharmaceutically acceptable composition thereof.

NEW COMPOUNDS

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Page/Page column 106, (2008/06/13)

This invention relates to novel compounds having the structural formula I below: and to their pharmaceutically acceptable salt, compositions and methods of use. These novel compounds provide a treatment or prophylaxis of cognitive impairment, Alzheimer Disease, neurodegeneration and dementia.

Imidazole derivatives

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, (2008/06/13)

Novel imidazole derivatives are disclosed. These compounds have a good affinity to the NMDA (N-methyl-D-aspartate)-receptor subtype selective blockers, which have a key function in modulating neuronal activity and plasticity which makes them key players in mediating processes underlying development of CNS as well as learning and memory formation. These compounds are useful in the control or treatment of diseases mediated by this receptor.

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