2-(1-Trityl-4-imidazolyl)benzaldehyde

95%

Reagent Code: #242822
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CAS Number 1402838-08-7

science Other reagents with same CAS 1402838-08-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 414.5 g/mol
Formula C₂₉H₂₂N₂O
badge Registry Numbers
MDL Number MFCD29059355
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of histamine H3 receptor antagonists. It plays a key role in constructing imidazole-containing drug candidates aimed at treating neurological disorders such as Alzheimer's disease, epilepsy, and sleep disorders. The trityl-protected imidazole group allows for selective reactivity during multi-step organic syntheses, making it valuable in medicinal chemistry for building complex molecules with high purity and yield.

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Test Parameter Specification
Appearance Off-White Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,880.00
inventory 250mg
10-20 days ฿7,400.00
inventory 1g
10-20 days ฿16,330.00
inventory 5g
10-20 days ฿47,610.00

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2-(1-Trityl-4-imidazolyl)benzaldehyde
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of histamine H3 receptor antagonists. It plays a key role in constructing imidazole-containing drug candidates aimed at treating neurological disorders such as Alzheimer's disease, epilepsy, and sleep disorders. The trityl-protected imidazole group allows for selective reactivity during multi-step organic syntheses, making it valuable in medicinal chemistry for building complex molecules with high purity

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of histamine H3 receptor antagonists. It plays a key role in constructing imidazole-containing drug candidates aimed at treating neurological disorders such as Alzheimer's disease, epilepsy, and sleep disorders. The trityl-protected imidazole group allows for selective reactivity during multi-step organic syntheses, making it valuable in medicinal chemistry for building complex molecules with high purity and yield.

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