(S)-2-Amino-2-(4-iodophenyl)ethan-1-ol hydrochloride

95%

Reagent Code: #36514
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CAS Number 2376106-42-0

science Other reagents with same CAS 2376106-42-0

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scatter_plot Molecular Information
Weight 299.5365 g/mol
Formula C₈H₁₁ClINO
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MDL Number MFCD18375926
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description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive molecules, particularly those targeting neurological and psychiatric disorders. Its structure, featuring an amino group and an iodophenyl moiety, makes it valuable for developing ligands that interact with specific receptors in the brain. Additionally, it is employed in the preparation of radiolabeled compounds for imaging studies, aiding in the investigation of biochemical pathways and drug distribution in the body. Its chiral nature also allows for the study of enantioselective interactions in drug development.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,990.00
inventory 100mg
10-20 days ฿2,450.00
inventory 1g
10-20 days ฿23,780.00
inventory 250mg
10-20 days ฿5,980.00

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(S)-2-Amino-2-(4-iodophenyl)ethan-1-ol hydrochloride
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive molecules, particularly those targeting neurological and psychiatric disorders. Its structure, featuring an amino group and an iodophenyl moiety, makes it valuable for developing ligands that interact with specific receptors in the brain. Additionally, it is employed in the preparation of radiolabeled compounds for imaging studies, aidi

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive molecules, particularly those targeting neurological and psychiatric disorders. Its structure, featuring an amino group and an iodophenyl moiety, makes it valuable for developing ligands that interact with specific receptors in the brain. Additionally, it is employed in the preparation of radiolabeled compounds for imaging studies, aiding in the investigation of biochemical pathways and drug distribution in the body. Its chiral nature also allows for the study of enantioselective interactions in drug development.

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