2-(Tetrahydropyran-4-yloxy)benzaldehyde

97%

Reagent Code: #132720
fingerprint
CAS Number 898289-31-1

science Other reagents with same CAS 898289-31-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.24 g/mol
Formula C₁₂H₁₄O₃
badge Registry Numbers
MDL Number MFCD09064958
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its aldehyde functional group allows for easy modification through reactions such as condensation, reduction, or nucleophilic addition, making it valuable in constructing complex organic structures. Commonly employed in medicinal chemistry for building blocks in the design of kinase inhibitors and central nervous system agents. Also utilized in the preparation of chiral compounds for asymmetric synthesis. Its tetrahydropyranyl moiety can act as a protecting group or influence solubility and stability in synthetic pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿25,570.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(Tetrahydropyran-4-yloxy)benzaldehyde
No image available

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its aldehyde functional group allows for easy modification through reactions such as condensation, reduction, or nucleophilic addition, making it valuable in constructing complex organic structures. Commonly employed in medicinal chemistry for building blocks in the design of kinase inhibitors and central nervous system agents. Also utilized in the preparation of chiral

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its aldehyde functional group allows for easy modification through reactions such as condensation, reduction, or nucleophilic addition, making it valuable in constructing complex organic structures. Commonly employed in medicinal chemistry for building blocks in the design of kinase inhibitors and central nervous system agents. Also utilized in the preparation of chiral compounds for asymmetric synthesis. Its tetrahydropyranyl moiety can act as a protecting group or influence solubility and stability in synthetic pathways.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...