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(4-[(TERT-BUTOXYCARBONYL)AMINO]PYRIDIN-3-YL)BORONIC ACID, with the molecular formula C14H19BN2O4, is a versatile chemical compound used extensively in organic synthesis and pharmaceutical research. It is recognized for its role as a reagent in the Suzuki-Miyaura cross-coupling reaction, a method pivotal for creating carbon-carbon bonds. (4-[(TERT-BUTOXYCARBONYL)AMINO]PYRIDIN-3-YL)BORONIC ACID's boronic acid functional group is notable for its capacity to form reversible covalent bonds with diols and other Lewis bases, which extends its utility in sensor development and drug delivery systems. As a building block for synthesizing biologically active molecules, including potential drugs and agrochemicals, (4-[(TERT-BUTOXYCARBONYL)AMINO]PYRIDIN-3-YL)BORONIC ACID holds significant value in both academic and industrial research.

863752-59-4

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863752-59-4 Usage

Uses

Used in Organic Synthesis:
(4-[(TERT-BUTOXYCARBONYL)AMINO]PYRIDIN-3-YL)BORONIC ACID is used as a reagent for the Suzuki-Miyaura cross-coupling reaction, facilitating the formation of carbon-carbon bonds, which is crucial for creating complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (4-[(TERT-BUTOXYCARBONYL)AMINO]PYRIDIN-3-YL)BORONIC ACID is used as a building block for the synthesis of biologically active molecules, contributing to the development of potential drugs and agrochemicals.
Used in Sensor Development:
(4-[(TERT-BUTOXYCARBONYL)AMINO]PYRIDIN-3-YL)BORONIC ACID's boronic acid functional group is utilized in sensor development due to its ability to form reversible covalent bonds with diols and other Lewis bases, enabling the detection and measurement of specific analytes.
Used in Drug Delivery Systems:
(4-[(TERT-BUTOXYCARBONYL)AMINO]PYRIDIN-3-YL)BORONIC ACID is employed in the design of drug delivery systems, where its capacity to form reversible bonds can be leveraged to control the release and targeting of therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 863752-59-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,7,5 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 863752-59:
(8*8)+(7*6)+(6*3)+(5*7)+(4*5)+(3*2)+(2*5)+(1*9)=204
204 % 10 = 4
So 863752-59-4 is a valid CAS Registry Number.

863752-59-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-[(2-methylpropan-2-yl)oxycarbonylamino]pyridin-3-yl]boronic acid

1.2 Other means of identification

Product number -
Other names (4-[(TERT-BUTOXYCARBONYL)AMINO]PYRIDIN-3-YL)BORONIC ACID

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:863752-59-4 SDS

863752-59-4Relevant academic research and scientific papers

Ring Closing and Related Methods and Intermediates

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Page/Page column 29, (2011/11/12)

Methods and intermediates useful for making compounds of the formula: and the preparation of compounds of Formula I, preferably including the formation of intermediate compounds of the formula:

SUBSTITUTED TETRAHYDROIMIDAZONAPHTHYRIDINES AND METHODS

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Page/Page column 54, (2010/11/29)

6,7,8,9-Tetrahydro-1H-imidazo[4,5-c]naphthyridines with a substituent at the 6-, 7-, 8-, or 9-position nitrogen atom, pharmaceutical compositions containing these compounds, methods of making the compounds, intermediates, and methods of use of these compo

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