CAS 872054-59-6 6-Methoxypyridine-2-boronic acid N-phenyldiethanolamine ester

NAVIGATION

6-Methoxypyridine-2-boronic acid N-phenyldiethanolamine ester

PRICE INQUIRY

Catalog Number

ACM872054596-1

CAS Number

872054-59-6

Product Name

6-Methoxypyridine-2-boronic acid N-phenyldiethanolamine ester

Structure

Category

Salt

Synonyms

6-Methoxypyridine-2-boronic acid N-phenyldiethanolamine ester, 6-Methoxy-2-pyridineboronic acid-N-phenyldiethanolamine ester, 872054-59-6, SureCN1526486, 649155_ALDRICH, ACN-S001309, AKOS015851994

IUPAC Name

2-(6-methoxypyridin-2-yl)-6-phenyl-1,3,6,2-dioxazaborocane

Molecular Weight

298.14

Molecular Formula

C₁₆H₁₉BN₂O₃

Canonical SMILES

B1(OCCN(CCO1)C2=CC=CC=C2)C3=NC(=CC=C3)OC

InChI Key

DBLBCHOTUMUCCT-UHFFFAOYSA-N

Melting Point

210ºC (dec.)(lit.)

Purity

96%

Application

The purpose of 6-Methoxypyridine-2-boronic acid N-phenyldiethanolamine ester is to serve as a versatile reactant in various chemical syntheses. It is utilized in the preparation of a range of compounds including alkylated sulfonamides through the alkylation of alcohols with an Ag/Mo hybrid catalyst, as well as 7-disubstituted oxyindoles which act as EP3 receptor antagonists. This compound also facilitates the synthesis of N-substituted sulfonamides via ferrous chloride-catalyzed N-alkylation using benzylic alcohols. Additionally, it supports the production of (alkyl)hydroxybenzimidazoles through an O- to N-acyl transfer reaction, functioning as key intermediates for EP3 receptor antagonists. Lastly, it aids in the creation of N-arylsulfonyl β-[(aryloxy)indolyl]acrylamides, which are potent and selective EP3 receptor antagonists.

Exact Mass

298.14900

Hazard Statements

Xi: Irritant;

Safety Description

26-36

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