H-D-HoPro-OMe.HCl

95%

Reagent Code: #113612
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CAS Number 18650-38-9

science Other reagents with same CAS 18650-38-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.65 g/mol
Formula C₇H₁₄ClNO₂
badge Registry Numbers
MDL Number MFCD00237412
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound, H-D-HoPro-OMe.HCl, is a protected form of D-hydroxyproline primarily utilized in peptide synthesis. It serves as a building block in the creation of complex peptides, with the methyl ester protecting the carboxyl group to ensure the hydroxyproline residue remains intact during the synthesis process. Its application is crucial in pharmaceutical research, where it aids in the development of peptide-based drugs. Additionally, it is used in biochemical studies to explore peptide structure and function, contributing to advancements in understanding protein interactions and enzymatic activities.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿297.00
inventory 1g
10-20 days ฿720.00

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H-D-HoPro-OMe.HCl
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This compound, H-D-HoPro-OMe.HCl, is a protected form of D-hydroxyproline primarily utilized in peptide synthesis. It serves as a building block in the creation of complex peptides, with the methyl ester protecting the carboxyl group to ensure the hydroxyproline residue remains intact during the synthesis process. Its application is crucial in pharmaceutical research, where it aids in the development of peptide-based drugs. Additionally, it is used in biochemical studies to explore peptide structure and

This compound, H-D-HoPro-OMe.HCl, is a protected form of D-hydroxyproline primarily utilized in peptide synthesis. It serves as a building block in the creation of complex peptides, with the methyl ester protecting the carboxyl group to ensure the hydroxyproline residue remains intact during the synthesis process. Its application is crucial in pharmaceutical research, where it aids in the development of peptide-based drugs. Additionally, it is used in biochemical studies to explore peptide structure and function, contributing to advancements in understanding protein interactions and enzymatic activities.

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