2-(2-Methyl-1H-imidazol-1-yl)acetic acid hydrochloride

95%

Reagent Code: #210475
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CAS Number 30163-87-2

science Other reagents with same CAS 30163-87-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.60 g/mol
Formula C₆H₉ClN₂O₂
badge Registry Numbers
MDL Number MFCD06801036
inventory_2 Storage & Handling
Storage Room temperature, inert atmosphere

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of histamine H3 receptor antagonists and other central nervous system agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for developing compounds with potential cognitive-enhancing or neuroprotective effects. It is also employed in the preparation of imidazole-containing bioactive molecules, where the acetic acid side chain facilitates conjugation or further chemical modification. Commonly found in research settings for drug discovery and development.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿40,640.00
2-(2-Methyl-1H-imidazol-1-yl)acetic acid hydrochloride
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Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of histamine H3 receptor antagonists and other central nervous system agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for developing compounds with potential cognitive-enhancing or neuroprotective effects. It is also employed in the preparation of imidazole-containing bioactive molecules, where the acetic acid side chain facilitates conjugation or fur

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of histamine H3 receptor antagonists and other central nervous system agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for developing compounds with potential cognitive-enhancing or neuroprotective effects. It is also employed in the preparation of imidazole-containing bioactive molecules, where the acetic acid side chain facilitates conjugation or further chemical modification. Commonly found in research settings for drug discovery and development.

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