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4-Ethoxy-2-formylphenylboronic acid, a boronic acid derivative with the molecular formula C10H11BO4, is a chemical compound that features an ethoxy group and a formyl group attached to a phenyl ring. It is widely recognized for its reactivity in boron-mediated processes, which makes it a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and materials.

1106867-72-4

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1106867-72-4 Usage

Uses

Used in Organic Chemistry:
4-Ethoxy-2-formylphenylboronic acid is used as a building block for the synthesis of various compounds in the field of organic chemistry. Its ability to react with a range of organic compounds through boron-mediated processes allows for the creation of functionalized molecules, which are essential in developing new pharmaceuticals and agrochemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Ethoxy-2-formylphenylboronic acid is used as a key intermediate in the synthesis of drugs. Its unique chemical properties enable the production of molecules with specific therapeutic effects, contributing to the development of innovative medications.
Used in Agrochemical Industry:
4-Ethoxy-2-formylphenylboronic acid is also utilized in the agrochemical industry as a precursor for the synthesis of pesticides and other crop protection agents. Its reactivity allows for the creation of molecules with targeted effects on pests and diseases, enhancing crop yields and quality.
Used in Material Science:
In the field of material science, 4-Ethoxy-2-formylphenylboronic acid is used in the development of new materials and catalysts. Its unique chemical properties make it a promising candidate for the creation of advanced materials with specific properties, such as improved conductivity, strength, or catalytic activity.
Used in Catalyst Development:
4-Ethoxy-2-formylphenylboronic acid is used as a component in the development of new catalysts. Its ability to participate in boron-mediated reactions makes it a valuable asset in designing catalysts that can efficiently facilitate various chemical processes, leading to more sustainable and efficient industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1106867-72-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,6,8,6 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1106867-72:
(9*1)+(8*1)+(7*0)+(6*6)+(5*8)+(4*6)+(3*7)+(2*7)+(1*2)=154
154 % 10 = 4
So 1106867-72-4 is a valid CAS Registry Number.

1106867-72-4SDS

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 (4-Ethoxy-2-formylphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names 4-Ethoxy-2-formylphenylboronic 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:1106867-72-4 SDS

1106867-72-4Downstream Products

1106867-72-4Relevant academic research and scientific papers

Design and enantioselective synthesis of 3-(α-acrylic acid) benzoxaboroles to combat carbapenemase resistance

Chen, Fener,Chen, Xiao-Pan,Deng, Ji,Li, Gen,Li, Guo-Bo,Schofield, Christopher J.,Xiao, You-Cai,Yan, Yu-Hang,Yu, Jun-Lin,Zhu, Kai-Rong,Brem, Jürgen

supporting information, p. 7709 - 7712 (2021/08/09)

Chiral 3-substituted benzoxaboroles were designed as carbapenemase inhibitors and efficiently synthesisedviaasymmetric Morita-Baylis-Hillman reaction. Some of the benzoxaboroles were potent inhibitors of clinically relevant carbapenemases and restored the activity of meropenem in bacteria harbouring these enzymes. Crystallographic analyses validate the proposed mechanism of binding to carbapenemases,i.e.in a manner relating to their antibiotic substrates. The results illustrate how combining a structure-based design approach with asymmetric catalysis can efficiently lead to potent β-lactamase inhibitors and provide a starting point to develop drugs combatting carbapenemases.

Design, Synthesis, and Characterization of Ogerin-Based Positive Allosteric Modulators for G Protein-Coupled Receptor 68 (GPR68)

Yu, Xufen,Huang, Xi-Ping,Kenakin, Terry P.,Slocum, Samuel T.,Chen, Xin,Martini, Michael L.,Liu, Jing,Jin, Jian

, p. 7557 - 7574 (2019/09/09)

G protein-coupled receptor 68 (GPR68) is an understudied orphan G protein-coupled receptor (GPCR). It is expressed most abundantly in the brain, potentially playing important roles in learning and memory. Pharmacological studies with GPR68 have been hinde

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