4-Amino-3-methoxycarbonylphenylboronic Acid Pinacol Ester

≥97%

Reagent Code: #90252
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CAS Number 363185-87-9

science Other reagents with same CAS 363185-87-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.12 g/mol
Formula C₁₄H₂₀NO₄B
badge Registry Numbers
MDL Number MFCD16293749
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of protease inhibitors and other therapeutic agents. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This compound is also utilized in the preparation of biologically active compounds and in research focused on drug discovery and development. Its boronic ester functionality makes it valuable in the design of sensors and materials for detecting specific analytes.

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Test Parameter Specification
Appearance White to Off-White Powder
Purity (%) 97.0-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,524.00
inventory 5g
10-20 days ฿23,040.00

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4-Amino-3-methoxycarbonylphenylboronic Acid Pinacol Ester
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Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of protease inhibitors and other therapeutic agents. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This compound is also utilized in the preparation of biologically active compounds and in research focused on drug discovery and development. Its boronic ester functionality makes it valuable in the design of

Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of protease inhibitors and other therapeutic agents. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This compound is also utilized in the preparation of biologically active compounds and in research focused on drug discovery and development. Its boronic ester functionality makes it valuable in the design of sensors and materials for detecting specific analytes.

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