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4-(Morpholine)carboxamidophenylboronic acid, pinacol ester is a boronic acid derivative with a phenyl group and a morpholine ring. As a pinacol ester, it features a bicyclic ring system that offers stability and protection of the boronic acid functionality. This chemical compound is widely used in organic synthesis and drug discovery, serving as a valuable building block for the synthesis of various organic molecules. Its unique structure and reactivity make it an essential tool for medicinal and chemical research.

656239-38-2

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656239-38-2 Usage

Uses

Used in Pharmaceutical Industry:
4-(Morpholine)carboxamidophenylboronic acid, pinacol ester is used as a key intermediate in the development of boron-containing pharmaceuticals. Its boronic acid functionality allows for the formation of stable boron-carbon bonds, which are crucial in the synthesis of complex organic molecules with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 4-(Morpholine)carboxamidophenylboronic acid, pinacol ester is employed as a versatile building block for the synthesis of various organic molecules. Its reactivity and unique structure enable the formation of a wide range of compounds with diverse functional groups, making it a valuable asset in the development of new chemical entities.
Used in Drug Discovery:
4-(Morpholine)carboxamidophenylboronic acid, pinacol ester is utilized in drug discovery as a starting material for the synthesis of potential drug candidates. Its boronic acid functionality can be exploited to create novel bioactive molecules with improved pharmacological properties, such as enhanced potency, selectivity, and reduced side effects.
Used in Chemical Research:
In chemical research, 4-(Morpholine)carboxamidophenylboronic acid, pinacol ester serves as a valuable tool for studying the reactivity and properties of boronic acid derivatives. Its unique structure allows researchers to explore new reaction pathways and mechanisms, contributing to the advancement of synthetic chemistry and the development of innovative synthetic strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 656239-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,6,2,3 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 656239-38:
(8*6)+(7*5)+(6*6)+(5*2)+(4*3)+(3*9)+(2*3)+(1*8)=182
182 % 10 = 2
So 656239-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H24BNO4/c1-16(2)17(3,4)23-18(22-16)14-7-5-13(6-8-14)15(20)19-9-11-21-12-10-19/h5-8H,9-12H2,1-4H3

656239-38-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H28484)  4-(4-Morpholinylcarbonyl)benzeneboronic acid pinacol ester, 97%   

  • 656239-38-2

  • 1g

  • 1034.0CNY

  • Detail
  • Alfa Aesar

  • (H28484)  4-(4-Morpholinylcarbonyl)benzeneboronic acid pinacol ester, 97%   

  • 656239-38-2

  • 5g

  • 3334.0CNY

  • Detail
  • Aldrich

  • (677809)  4-(Morpholine-4-carbonyl)phenylboronicacidpinacolester  97%

  • 656239-38-2

  • 677809-1G

  • 944.19CNY

  • Detail
  • Aldrich

  • (677809)  4-(Morpholine-4-carbonyl)phenylboronicacidpinacolester  97%

  • 656239-38-2

  • 677809-5G

  • 2,937.87CNY

  • Detail

656239-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name morpholin-4-yl-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanone

1.2 Other means of identification

Product number -
Other names -

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:656239-38-2 SDS

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