N-Methoxy-N,4-dimethyl-1-naphthamide

95%

Reagent Code: #215590
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CAS Number 1807542-90-0

science Other reagents with same CAS 1807542-90-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.27 g/mol
Formula C₁₄H₁₅NO₂
badge Registry Numbers
MDL Number MFCD28134514
thermostat Physical Properties
Boiling Point 418.9±24.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.137±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. Its structure supports use in cross-coupling reactions and cyclization processes, making it valuable in the development of complex aromatic compounds. Commonly employed in research settings for constructing naphthalene-based frameworks found in certain therapeutic agents. Also utilized in the synthesis of fluorescent probes due to the inherent photophysical properties of the naphthalene core. Shows utility in medicinal chemistry for structure-activity relationship (SAR) studies, where the N-methoxy amide group acts as a stable amide isostere.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿7,150.00
250mg
10-20 days ฿12,170.00
N-Methoxy-N,4-dimethyl-1-naphthamide
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Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. Its structure supports use in cross-coupling reactions and cyclization processes, making it valuable in the development of complex aromatic compounds. Commonly employed in research settings for constructing naphthalene-based frameworks found in certain therapeutic agents. Also utilized in the synthesis of fluorescent probes due to the inherent photophysical properties of the naphthale

Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. Its structure supports use in cross-coupling reactions and cyclization processes, making it valuable in the development of complex aromatic compounds. Commonly employed in research settings for constructing naphthalene-based frameworks found in certain therapeutic agents. Also utilized in the synthesis of fluorescent probes due to the inherent photophysical properties of the naphthalene core. Shows utility in medicinal chemistry for structure-activity relationship (SAR) studies, where the N-methoxy amide group acts as a stable amide isostere.

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