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2-(Morpholino)phenylboronic acid pinacolate is a boronic acid compound that plays a significant role in organic synthesis and pharmaceutical research. It is characterized by the presence of a morpholino group, a heterocyclic amine, and a phenylboronic acid group. The pinacolate moiety, a large and sterically hindered ligand, contributes to the stability of the boron center and enhances its reactivity. 2-(MORPHOLINO)PHENYLBORONIC ACID PINACOLATE is particularly known for its applications in Suzuki-Miyaura cross-coupling reactions, which are crucial for the formation of carbon-carbon bonds in organic synthesis. Moreover, the morpholino group serves as a directing group for selective C-H activation reactions, making 2-(Morpholino)phenylboronic acid pinacolate a promising candidate in medicinal chemistry for the development of new drugs to combat various diseases.

1050505-83-3

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1050505-83-3 Usage

Uses

Used in Organic Synthesis:
2-(Morpholino)phenylboronic acid pinacolate is used as a reagent for Suzuki-Miyaura cross-coupling reactions, which are essential for the formation of carbon-carbon bonds in organic synthesis. Its pinacolate moiety provides stability and enhances the reactivity of the boron center, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(Morpholino)phenylboronic acid pinacolate is utilized as a key intermediate in the development of new drugs for various diseases. Its morpholino group acts as a directing group for selective C-H activation reactions, allowing for the targeted modification of specific molecular structures. This selective reactivity is crucial for the design of drugs with improved efficacy and reduced side effects.
Used in Medicinal Chemistry:
2-(Morpholino)phenylboronic acid pinacolate is employed as a building block in the synthesis of bioactive compounds with potential therapeutic applications. Its unique structural features and reactivity make it a versatile component in the design and synthesis of novel pharmaceutical agents, contributing to the advancement of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 1050505-83-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,0,5,0 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1050505-83:
(9*1)+(8*0)+(7*5)+(6*0)+(5*5)+(4*0)+(3*5)+(2*8)+(1*3)=103
103 % 10 = 3
So 1050505-83-3 is a valid CAS Registry Number.

1050505-83-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

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

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

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More Details:1050505-83-3 SDS

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