H-DL-Val-OEt.HCl

98%

Reagent Code: #116245
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CAS Number 23358-42-1

science Other reagents with same CAS 23358-42-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 181.66 g/mol
Formula C₇H₁₆ClNO₂
badge Registry Numbers
MDL Number MFCD00067542
thermostat Physical Properties
Melting Point 94°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used as a building block in peptide synthesis, particularly for introducing valine residues into peptide chains. It is also employed in the preparation of modified amino acids and peptide derivatives for biochemical research. The compound is utilized in the development of pharmaceuticals, especially in the synthesis of drugs that target specific enzymes or receptors. Additionally, it serves as a precursor in the production of chiral compounds for asymmetric synthesis. Its ester group makes it suitable for applications requiring solubility in organic solvents, facilitating reactions in non-aqueous environments.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿2,637.00
inventory 5g
10-20 days ฿603.00

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H-DL-Val-OEt.HCl
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Used as a building block in peptide synthesis, particularly for introducing valine residues into peptide chains. It is also employed in the preparation of modified amino acids and peptide derivatives for biochemical research. The compound is utilized in the development of pharmaceuticals, especially in the synthesis of drugs that target specific enzymes or receptors. Additionally, it serves as a precursor in the production of chiral compounds for asymmetric synthesis. Its ester group makes it suitable fo

Used as a building block in peptide synthesis, particularly for introducing valine residues into peptide chains. It is also employed in the preparation of modified amino acids and peptide derivatives for biochemical research. The compound is utilized in the development of pharmaceuticals, especially in the synthesis of drugs that target specific enzymes or receptors. Additionally, it serves as a precursor in the production of chiral compounds for asymmetric synthesis. Its ester group makes it suitable for applications requiring solubility in organic solvents, facilitating reactions in non-aqueous environments.

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