Fmoc-Dab(ivDde)-OH

98%

Reagent Code: #66187
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CAS Number 607366-21-2

science Other reagents with same CAS 607366-21-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 546.65 g/mol
Formula C₃₂H₃₈N₂O₆
badge Registry Numbers
MDL Number MFCD01631660
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This compound is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a building block for the introduction of the amino acid Dab (diaminobutyric acid) into peptide chains. The Fmoc (9-fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino group, while the ivDde (1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl) group protects the side chain amine of Dab. This dual protection allows for selective deprotection, enabling the synthesis of complex peptides with specific modifications. It is especially useful in the preparation of peptides for research in biochemistry, pharmaceuticals, and drug development.

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inventory 250mg
10-20 days ฿3,078.00

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Fmoc-Dab(ivDde)-OH
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This compound is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a building block for the introduction of the amino acid Dab (diaminobutyric acid) into peptide chains. The Fmoc (9-fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino group, while the ivDde (1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl) group protects the side chain amine of Dab. This dual protection allows for selective deprotection, enabling t

This compound is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a building block for the introduction of the amino acid Dab (diaminobutyric acid) into peptide chains. The Fmoc (9-fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino group, while the ivDde (1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl) group protects the side chain amine of Dab. This dual protection allows for selective deprotection, enabling the synthesis of complex peptides with specific modifications. It is especially useful in the preparation of peptides for research in biochemistry, pharmaceuticals, and drug development.

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