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2-Morpholinopyridine-3-boronic acid, pinacol ester is a boronic acid derivative characterized by its versatile functional group and pinacol ester moiety. It serves as a valuable building block in organic synthesis, facilitating the formation of carbon-carbon bonds through Suzuki-Miyaura coupling reactions. 2-Morpholinopyridine-3-boronic acid, pinacol ester's unique structure, which includes a boronic acid group for covalent bond formation and a pinacol ester group for enhanced stability and solubility, makes it a preferred reagent in various organic transformations.

1150561-72-0

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1150561-72-0 Usage

Uses

Used in Organic Synthesis:
2-Morpholinopyridine-3-boronic acid, pinacol ester is used as a building block for the synthesis of complex organic molecules, particularly in the formation of carbon-carbon bonds through Suzuki-Miyaura coupling reactions. Its boronic acid functional group allows for versatile covalent bond formation with other molecules, making it a valuable tool in creating a wide range of organic compounds.
Used in Medicinal and Agrochemical Research:
In the fields of medicinal and agrochemical research, 2-Morpholinopyridine-3-boronic acid, pinacol ester is utilized as a reagent for the synthesis of bioactive compounds. Its ability to form stable covalent bonds with various molecular structures contributes to the development of new pharmaceuticals and agrochemicals with improved efficacy and selectivity.
Used in Pharmaceutical Industry:
2-Morpholinopyridine-3-boronic acid, pinacol ester is employed in the pharmaceutical industry as a key intermediate in the synthesis of bioactive compounds. Its unique structure and reactivity make it a preferred choice for the development of new drugs with potential therapeutic applications. The pinacol ester group also provides enhanced solubility, which is crucial for the drug's bioavailability and pharmacokinetic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1150561-72-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,0,5,6 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1150561-72:
(9*1)+(8*1)+(7*5)+(6*0)+(5*5)+(4*6)+(3*1)+(2*7)+(1*2)=120
120 % 10 = 0
So 1150561-72-0 is a valid CAS Registry Number.

1150561-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)morpholine

1.2 Other means of identification

Product number -
Other names 4-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]morpholine

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:1150561-72-0 SDS

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