(4R)-3-[(9H-Fluoren-9-ylmethoxy)carbonyl]-1,3-thiazolane-4-carboxylic acid

≥90%

Reagent Code: #231911
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CAS Number 423719-54-4

science Other reagents with same CAS 423719-54-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 355.41 g/mol
Formula C₁₉H₁₇NO₄S
badge Registry Numbers
MDL Number MFCD00235910
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in peptide synthesis as a protected intermediate, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethyloxycarbonyl (Fmoc) group acts as a temporary protecting group for the amine function, allowing selective deprotection under mild basic conditions without affecting other sensitive parts of the molecule. The thiazolane ring provides structural rigidity and can serve as a proline mimic or a scaffold in peptidomimetic drug design. This compound is valuable in the preparation of modified peptides with enhanced stability or biological activity, commonly used in pharmaceutical research and development of bioactive molecules.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿7,380.00
(4R)-3-[(9H-Fluoren-9-ylmethoxy)carbonyl]-1,3-thiazolane-4-carboxylic acid
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Used in peptide synthesis as a protected intermediate, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethyloxycarbonyl (Fmoc) group acts as a temporary protecting group for the amine function, allowing selective deprotection under mild basic conditions without affecting other sensitive parts of the molecule. The thiazolane ring provides structural rigidity and can serve as a proline mimic or a scaffold in peptidomimetic drug design. This compound is valuable in the preparation of mod

Used in peptide synthesis as a protected intermediate, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethyloxycarbonyl (Fmoc) group acts as a temporary protecting group for the amine function, allowing selective deprotection under mild basic conditions without affecting other sensitive parts of the molecule. The thiazolane ring provides structural rigidity and can serve as a proline mimic or a scaffold in peptidomimetic drug design. This compound is valuable in the preparation of modified peptides with enhanced stability or biological activity, commonly used in pharmaceutical research and development of bioactive molecules.

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