4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-methyl-1H-pyrrole-2-carboxylic acid

98%

Reagent Code: #104575
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CAS Number 195387-29-2

science Other reagents with same CAS 195387-29-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 362.38 g/mol
Formula C₂₁H₁₈N₂O₄
badge Registry Numbers
MDL Number MFCD02094546
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

description Product Description

This compound, 4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-methyl-1H-pyrrole-2-carboxylic acid, is a specialized Fmoc-protected building block used in solid-phase peptide synthesis (SPPS). The Fmoc group protects the amino group at the 4-position of the 1-methylpyrrole ring, enabling controlled incorporation of the pyrrole-2-carboxylic acid moiety into peptide chains. It prevents unwanted side reactions during coupling steps and can be selectively removed under mild basic conditions, such as with piperidine. This reagent is essential for synthesizing complex peptides containing non-natural pyrrole units, with applications in medicinal chemistry, drug discovery, and biochemical research.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿11,700.00
100mg
10-20 days ฿7,200.00
1g
10-20 days ฿24,804.00
4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-methyl-1H-pyrrole-2-carboxylic acid
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This compound, 4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-methyl-1H-pyrrole-2-carboxylic acid, is a specialized Fmoc-protected building block used in solid-phase peptide synthesis (SPPS). The Fmoc group protects the amino group at the 4-position of the 1-methylpyrrole ring, enabling controlled incorporation of the pyrrole-2-carboxylic acid moiety into peptide chains. It prevents unwanted side reactions during coupling steps and can be selectively removed under mild basic conditions, such as with pip

This compound, 4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-methyl-1H-pyrrole-2-carboxylic acid, is a specialized Fmoc-protected building block used in solid-phase peptide synthesis (SPPS). The Fmoc group protects the amino group at the 4-position of the 1-methylpyrrole ring, enabling controlled incorporation of the pyrrole-2-carboxylic acid moiety into peptide chains. It prevents unwanted side reactions during coupling steps and can be selectively removed under mild basic conditions, such as with piperidine. This reagent is essential for synthesizing complex peptides containing non-natural pyrrole units, with applications in medicinal chemistry, drug discovery, and biochemical research.

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