914397-31-2

Usage

Uses

Used in Pharmaceutical Research and Development:
3-(N-Cyclopropylaminocarbonyl)phenylboronic acid, pinacol ester is used as a key intermediate for the synthesis of biologically active molecules in the pharmaceutical industry. Its unique boronic acid group allows for the formation of stable and selective complexes, which is crucial for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Research and Development:
In the agrochemical industry, 3-(N-Cyclopropylaminocarbonyl)phenylboronic acid, pinacol ester is employed as a key intermediate in the synthesis of biologically active molecules for crop protection and pest control. Its ability to form stable complexes with various compounds makes it a valuable tool in the development of novel agrochemicals with enhanced performance and selectivity.
Used in Organic Synthesis:
3-(N-Cyclopropylaminocarbonyl)phenylboronic acid, pinacol ester is used as a reagent in the Suzuki-Miyaura coupling reaction, a widely employed method for the formation of carbon-carbon bonds in organic synthesis. Its boronic acid group enables the formation of stable and selective complexes, making it an essential component in the synthesis of various organic compounds.
Used in the Synthesis of Biologically Active Molecules:
3-(N-Cyclopropylaminocarbonyl)phenylboronic acid, pinacol ester is used as a building block in the synthesis of biologically active molecules, such as pharmaceuticals and agrochemicals. Its unique chemical properties and reactivity make it a versatile and valuable intermediate in the development of new and improved compounds with potential therapeutic and agricultural applications.

InChI:InChI=1/C16H22BNO3/c1-15(2)16(3,4)21-17(20-15)12-7-5-6-11(10-12)14(19)18-13-8-9-13/h5-7,10,13H,8-9H2,1-4H3,(H,18,19)

Upstream product

• 337535-74-7 3-bromo-N-cyclopropylbenzamide 
• 73183-34-3 bis(pinacol)diborane 
• 1711-09-7 3-bromobenzoyl chloride 
• 585-76-2 m-bromobenzoic acid 

Downstream Products

• 1051935-57-9 C₂₁H₂₂N₂O₂ 

Relevant academic research and scientific papers

Design, synthesis and biological evaluation of 1H-indazole derivatives as novel ASK1 inhibitors

Apoptosis signal-regulating kinase 1 (ASK1, MAP3K5), a member of the mitogen-activated protein kinase (MAPK) signaling pathway, is involved in cell survival, differentiation, stress response, and apoptosis. ASK1 kinase inhibition has emerged as a promisin

ASK1 inhibitor, derivative, preparation method, pharmaceutical composition and application thereof

The invention discloses an ASK1 inhibitor, a derivative, a preparation method, a pharmaceutical composition and application thereof. The structure of the compound is shown as a formula I. The ASK1 inhibitor derivative relates to an isomer, a diastereoisom

PYRIDOPYRIMIDINE COMPOUNDS ACTING AS MTORC 1/2 DOUBLE-KINASE INHIBITORS

Disclosed are a series of pyridopyrimidine compounds and a use of same in the preparation of drugs associated with mTORC 1/2 dual complex inhibitors, and specifically disclosed is a use of the compounds as shown in formula (IV), tautomers thereof or pharmaceutically acceptable salts thereof in the preparation of drugs associated with mTORC 1/2 dual complex inhibitors.

New substituted spiro[cycloalkyl-1,3'-indo]-2'(1'H)-one derivatives and their use as p38 mitogen-activated kinase inhibitors

This invention is directed to new inhibitors of the p38 mitogen-activated protein kinase having the general formula (I) to processes for their preparation; to pharmaceutical compositions comprising them; and to their use in therapy.

ANTI-VIRAL COMPOUNDS

Disclosed are compounds, stereoisomers, tautomers, pharmaceutically acceptable salts, or prodrugs thereof of having Formula (I), their preparation, use, and compositions thereof for treating an infection mediated at least in part by a virus in the Flavivi

2-AMINOQUINAZOLINE DERIVATIVES

2-Aminoquinazoline derivatives represented by the general formula (I) or pharmacologically acceptable salts thereof: (I) wherein R1 and R2 are each independently hydrogen, substituted or unsubstituted lower alkyl, or the like; X is a bond or CR7aR7b (wherein R7a and R7b are each independently hydrogen or the like); when X is a bond, R3 is substituted or unsubstituted aryl or a substituted or unsubstituted aromatic heterocyclic group, while when X is CR7aR7b, R3 is substituted or unsubstituted lower alkoxy, substituted or unsubstituted aryl, or the like; R4 is hydrogen, hydroxy, substituted or unsubstituted lower alkoxy, or the like; and R5 is hydrogen, substituted or unsubstituted aryl, or the like.