What is the molecular formula of 4-Ethoxyphenylboronic acid?

The molecular formula is C8H11BO3.

What is the synonym for 4-Ethoxyphenylboronic acid?

The synonym is 4-Ethoxybenzeneboronic Acid.

When was 4-Ethoxyphenylboronic acid created?

It was created on July 19, 2005.

What is the IUPAC name of 4-Ethoxyphenylboronic acid?

The IUPAC name is (4-ethoxyphenyl)boronic acid.

What is the InChI of 4-Ethoxyphenylboronic acid?

The InChI is InChI=1S/C8H11BO3/c1-2-12-8-5-3-7(4-6-8)9(10)11/h3-6,10-11H,2H2,1H3.

What is the InChIKey of 4-Ethoxyphenylboronic acid?

The InChIKey is WRQNDLDUNQMTCL-UHFFFAOYSA-N.

What is the canonical SMILES of 4-Ethoxyphenylboronic acid?

The canonical SMILES is B(C1=CC=C(C=C1)OCC)(O)O.

What is the molecular weight of 4-Ethoxyphenylboronic acid?

The molecular weight is 165.98 g/mol.

Is 4-Ethoxyphenylboronic acid canonicalized?

Yes, the compound is canonicalized.

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4-Ethoxyphenylboronic acid

Name: 4-Ethoxyphenylboronic acid
SKU: ACM22237134-2
Rating: 5 (1 reviews)

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Catalog NumberACM22237134-2

CAS Number22237-13-4

CategorySalt

Synonyms

RARECHEM AH PB 0138;P-ETHOXYPHENYLBORONIC ACID;4-ETHOXYPHENYLBORONIC ACID;4-ETHOXYBENZENEBORONIC ACID;AKOS BRN-0070;4-Ethoxybenzeneboronicacid,96%;4-Etoxyphenylboronic acid;4-Ethoxyphenylboronic Acid (contains varying amounts of Anhydride)

IUPAC Name

(4-ethoxyphenyl)boronic acid

Molecular Weight

165.98

Molecular Formula

C₈H₁₁BO₃

Canonical SMILES

B(C1=CC=C(C=C1)OCC)(O)O

InChI Key

WRQNDLDUNQMTCL-UHFFFAOYSA-N

Boiling Point

317.6ºC at 760 mmHg

Melting Point

121-128ºC

Flash Point

145.9ºC

Purity

98%

Density

1.13 g/cm³

Appearance

White crystalline powder

Application

4-Ethoxyphenylboronic acid serves as a key reactant in Suzuki cross-coupling reactions, enabling the synthesis of a diverse array of biologically active molecules. This white crystalline powder is instrumental in the development of novel compounds, such as modulators of survival motor neuron protein for the treatment of spinal muscular atrophy, amino-trimethoxyphenyl-aryl thiazoles with microtubule inhibiting and antitumor properties, and bicyclic hydroxyphenyl methanone derivatives that act as hydroxysteroid dehydrogenase inhibitors. Additionally, it facilitates the creation of dual immunosuppressive and anti-inflammatory agents, as well as antiproliferative compounds through Suzuki cross-coupling and amination reactions.

Exact Mass

166.08000

Hazard Statements

Xn:Harmful;

Safety Description

S26-S37/39

WGK Germany

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