Sigma Aldrich N-Boc-pyrrole

Catalog No.	Quantity
42-583-4100ML	100 mL
42-583-425ML	25 mL

Catalog No. 42-583-4100ML

Supplier: Sigma Aldrich 425834100ML

Description

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

• N-boc-pyrrole is an n-protected pyrrole. it undergoes diels-alder reaction with enantiomerically pure allene-1,3-dicarboxylates to form endo-adducts with retention in configurations at two newly generated stereogenic centers. it also undergoes cyclopropanation with methyl phenyldiazoacetate to form both monocyclopropane and dicyclopropane. its IR-catalyzed c-h borylation followed by cross coupling with 3-chlorothiophene to form biheterocycle has been reported.n-boc-pyrrole was used in the synthesis of 1-(tert-butoxycarbonyl)-1h-pyrrol-2-ylboronic acid by treating with n-buli and subsequent reaction with trimethyl borate.it may be used as starting material in the synthesis of the following:
• Tropane drivatives
• N-boc-2-(4-methoxyphenyl)pyrrole
• N-boc-pyrrol-2-ylboronic acid

Specifications

• CAS: 5176-27-2
• Density: 1 g/mL (at 25°C (literature))
• Boiling Point: 91°C to 92°C (20 mmHg)
• Molecular Formula: C9H13NO2
• Refractive Index: n20/D 1.4685 (literature)
• Linear Formula: C9H13NO2
• MDL Number: MFCD00209559
• Quantity: 100 mL
• Synonym: tert-Butyl 1-pyrrolecarboxylate
• Molecular Weight (g/mol): 167.21
• Percent Purity: 98%
• Biological Activity: Respiratory System