(S)-Methyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-imidazol-4-yl)propanoate

95%

Reagent Code: #233341
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CAS Number 160450-10-2

science Other reagents with same CAS 160450-10-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 391.42 g/mol
Formula C₂₂H₂₁N₃O₄
badge Registry Numbers
MDL Number MFCD27578253
thermostat Physical Properties
Melting Point 113-115 °C
Boiling Point 671.6±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.303±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

(S)-Fmoc-histidine methyl ester is a protected derivative of L-histidine, featuring an Fmoc group on the α-amino group and a methyl ester on the carboxylic acid. It serves as a key building block in solution-phase peptide synthesis, enabling selective protection and stepwise assembly of peptide chains. The Fmoc moiety allows for mild basic deprotection, while the methyl ester protects the C-terminus, facilitating orthogonal deprotection strategies. After ester hydrolysis, it can be incorporated into solid-phase synthesis. Its defined stereochemistry maintains chiral purity, making it ideal for producing custom peptides, peptide analogs, and research compounds in biochemical and pharmaceutical applications, such as enzyme inhibitors or antimicrobial agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,730.00
inventory 250mg
10-20 days ฿4,630.00
inventory 1g
10-20 days ฿12,470.00
(S)-Methyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-imidazol-4-yl)propanoate
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(S)-Fmoc-histidine methyl ester is a protected derivative of L-histidine, featuring an Fmoc group on the α-amino group and a methyl ester on the carboxylic acid. It serves as a key building block in solution-phase peptide synthesis, enabling selective protection and stepwise assembly of peptide chains. The Fmoc moiety allows for mild basic deprotection, while the methyl ester protects the C-terminus, facilitating orthogonal deprotection strategies. After ester hydrolysis, it can be incorporated into soli

(S)-Fmoc-histidine methyl ester is a protected derivative of L-histidine, featuring an Fmoc group on the α-amino group and a methyl ester on the carboxylic acid. It serves as a key building block in solution-phase peptide synthesis, enabling selective protection and stepwise assembly of peptide chains. The Fmoc moiety allows for mild basic deprotection, while the methyl ester protects the C-terminus, facilitating orthogonal deprotection strategies. After ester hydrolysis, it can be incorporated into solid-phase synthesis. Its defined stereochemistry maintains chiral purity, making it ideal for producing custom peptides, peptide analogs, and research compounds in biochemical and pharmaceutical applications, such as enzyme inhibitors or antimicrobial agents.

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