N-(4,5-Dihydrothiazol-2-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

≥95%

Reagent Code: #215862
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CAS Number 2828440-28-2

science Other reagents with same CAS 2828440-28-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.23 g/mol
Formula C₁₆H₂₁BN₂O₃S
inventory_2 Storage & Handling
Density 1.22±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical research and development of novel therapeutic agents. Commonly employed in the preparation of protease inhibitors and anti-inflammatory agents due to its ability to incorporate into complex heterocyclic frameworks. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies, where the thiazoline and benzamide moieties contribute to target binding and molecular stability.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,880.00
250mg
10-20 days ฿3,180.00
1g
10-20 days ฿8,580.00
N-(4,5-Dihydrothiazol-2-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical research and development of novel therapeutic agents. Commonly employed in the preparation of protease inhibitors and anti-inflammatory agents due to its ability to incorporate into complex heterocyclic frameworks. Also utilized in medicinal chemistry for structure-activity re

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical research and development of novel therapeutic agents. Commonly employed in the preparation of protease inhibitors and anti-inflammatory agents due to its ability to incorporate into complex heterocyclic frameworks. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies, where the thiazoline and benzamide moieties contribute to target binding and molecular stability.

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