4-Bromobenzenecarboximidamide Hydrochloride

≥96%

Reagent Code: #78261
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CAS Number 22265-36-7

science Other reagents with same CAS 22265-36-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.5 g/mol
Formula C₇H₈BrClN₂
thermostat Physical Properties
Boiling Point 260.8ºC
inventory_2 Storage & Handling
Density 1.62g/cm3
Storage room temperature, dry

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals. It is particularly valuable in the development of drugs targeting cardiovascular diseases and hypertension. Additionally, it plays a role in the synthesis of biologically active molecules and agrochemicals. Its reactivity makes it useful in cross-coupling reactions, aiding in the creation of complex organic structures. Researchers also utilize it in the study of enzyme inhibition and receptor binding mechanisms.

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inventory 1g
10-20 days ฿1,692.00

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4-Bromobenzenecarboximidamide Hydrochloride
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals. It is particularly valuable in the development of drugs targeting cardiovascular diseases and hypertension. Additionally, it plays a role in the synthesis of biologically active molecules and agrochemicals. Its reactivity makes it useful in cross-coupling reactions, aiding in the creation of complex organic structures. Researchers also utilize it in the study of enzyme inhibition

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals. It is particularly valuable in the development of drugs targeting cardiovascular diseases and hypertension. Additionally, it plays a role in the synthesis of biologically active molecules and agrochemicals. Its reactivity makes it useful in cross-coupling reactions, aiding in the creation of complex organic structures. Researchers also utilize it in the study of enzyme inhibition and receptor binding mechanisms.

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