(S)-2-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(tert-butoxy)-N-(2,4-dimethoxybenzyl)-4-oxobutanamido)acetic acid

95%

Reagent Code: #38120
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CAS Number 900152-72-9

science Other reagents with same CAS 900152-72-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 618.6700 g/mol
Formula C₃₄H₃₈N₂O₉
badge Registry Numbers
MDL Number MFCD10001337
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized in the field of peptide synthesis, where it serves as a key building block for constructing complex peptide sequences. Its structure includes protective groups, such as the Fmoc (9-fluorenylmethoxycarbonyl) group, which is widely used in solid-phase peptide synthesis (SPPS) to protect amino acids during the stepwise assembly of peptides. The tert-butoxy and dimethoxybenzyl groups further enhance its stability and selectivity in reactions, making it suitable for synthesizing peptides with specific functional or structural requirements. It is particularly valuable in the production of custom peptides for research, pharmaceuticals, and biotechnology applications, where precise control over peptide structure is essential.

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Test Parameter Specification
Appearance Off White Powder
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,375.00
inventory 1g
10-20 days ฿21,730.00
inventory 5g
10-20 days ฿80,000.00

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(S)-2-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(tert-butoxy)-N-(2,4-dimethoxybenzyl)-4-oxobutanamido)acetic acid
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This chemical is primarily utilized in the field of peptide synthesis, where it serves as a key building block for constructing complex peptide sequences. Its structure includes protective groups, such as the Fmoc (9-fluorenylmethoxycarbonyl) group, which is widely used in solid-phase peptide synthesis (SPPS) to protect amino acids during the stepwise assembly of peptides. The tert-butoxy and dimethoxybenzyl groups further enhance its stability and selectivity in reactions, making it suitable for synthesizing peptides with specific functional or structural requirements. It is particularly valuable in the production of custom peptides for research, pharmaceuticals, and biotechnology applications, where precise control over peptide structure is essential.
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