Methyl tetrahydro-2H-pyran-3-carboxylate

≥95%

Reagent Code: #208925
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CAS Number 18729-20-9

science Other reagents with same CAS 18729-20-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 144.17 g/mol
Formula C₇H₁₂O₃
badge Registry Numbers
MDL Number MFCD09839011
thermostat Physical Properties
Boiling Point 183°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. Its ester and cyclic ether functionalities make it suitable for transformations such as reductions, hydrolyses, and nucleophilic additions. Commonly employed in the preparation of bioactive molecules where a functionalized six-membered oxygen heterocycle is required. Also utilized in the development of chiral building blocks through asymmetric synthesis routes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿600.00
inventory 250mg
10-20 days ฿630.00
inventory 1g
10-20 days ฿1,280.00
inventory 5g
10-20 days ฿5,490.00
inventory 25g
10-20 days ฿18,910.00
Methyl tetrahydro-2H-pyran-3-carboxylate
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Used as an intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. Its ester and cyclic ether functionalities make it suitable for transformations such as reductions, hydrolyses, and nucleophilic additions. Commonly employed in the preparation of bioactive molecules where a functionalized six-membered oxygen heterocycle is required. Also utilized in the development of chiral building blocks through asymmetric synthesis routes.

Used as an intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. Its ester and cyclic ether functionalities make it suitable for transformations such as reductions, hydrolyses, and nucleophilic additions. Commonly employed in the preparation of bioactive molecules where a functionalized six-membered oxygen heterocycle is required. Also utilized in the development of chiral building blocks through asymmetric synthesis routes.

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