Methyl 3-nitrobenzylideneacetoacetate

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Reagent Code: #208619
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CAS Number 39562-17-9

science Other reagents with same CAS 39562-17-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.22 g/mol
Formula C₁₂H₁₁NO₅
badge Registry Numbers
MDL Number MFCD00142134
thermostat Physical Properties
Melting Point 158℃
Boiling Point 387℃
inventory_2 Storage & Handling
Density 1.296 g/cm3
Storage 2-8℃, dry, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of pyrazole derivatives which exhibit biological activity. It serves as a key building block in heterocyclic chemistry due to its α,β-unsaturated carbonyl structure, enabling Michael addition and cyclization reactions. Commonly applied in the development of dyes, fluorescent probes, and UV-absorbing compounds owing to its conjugated system. Also utilized in organic synthesis for constructing complex molecules through selective functional group transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,320.00
inventory 5g
10-20 days ฿3,570.00
inventory 25g
10-20 days ฿12,840.00
inventory 100g
10-20 days ฿40,910.00

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Methyl 3-nitrobenzylideneacetoacetate
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of pyrazole derivatives which exhibit biological activity. It serves as a key building block in heterocyclic chemistry due to its α,β-unsaturated carbonyl structure, enabling Michael addition and cyclization reactions. Commonly applied in the development of dyes, fluorescent probes, and UV-absorbing compounds owing to its conjugated system. Also utilized in organic synthesis for constructing comp

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of pyrazole derivatives which exhibit biological activity. It serves as a key building block in heterocyclic chemistry due to its α,β-unsaturated carbonyl structure, enabling Michael addition and cyclization reactions. Commonly applied in the development of dyes, fluorescent probes, and UV-absorbing compounds owing to its conjugated system. Also utilized in organic synthesis for constructing complex molecules through selective functional group transformations.

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