2-(Diisobutylamino)-2-phenylacetic acid hydrochloride

≥95%

Reagent Code: #73301
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CAS Number 1956310-34-1

science Other reagents with same CAS 1956310-34-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 299.84 g/mol
Formula C₁₆H₂₆ClNO₂
badge Registry Numbers
MDL Number MFCD28991762
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals. Its structure, featuring both amino and phenyl groups, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological and cardiovascular systems. Additionally, it is employed in research settings to study receptor interactions and enzyme inhibition, aiding in the discovery of new therapeutic agents. Its hydrochloride form enhances solubility, facilitating its use in aqueous reaction conditions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿45,153.00
inventory 100mg
10-20 days ฿18,090.00
inventory 250mg
10-20 days ฿34,704.00

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2-(Diisobutylamino)-2-phenylacetic acid hydrochloride
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This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals. Its structure, featuring both amino and phenyl groups, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological and cardiovascular systems. Additionally, it is employed in research settings to study receptor interactions and enzyme inhibition, aiding in the discovery of new therapeutic agents

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals. Its structure, featuring both amino and phenyl groups, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological and cardiovascular systems. Additionally, it is employed in research settings to study receptor interactions and enzyme inhibition, aiding in the discovery of new therapeutic agents. Its hydrochloride form enhances solubility, facilitating its use in aqueous reaction conditions.

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