ETHYL 6-OXASPIRO[2.5]OCTANE-1-CARBOXYLATE

95%

Reagent Code: #75980
fingerprint
CAS Number 909406-74-2

science Other reagents with same CAS 909406-74-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184 g/mol
Formula C₁₀H₁₆O₃
badge Registry Numbers
MDL Number MFCD23105848
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile intermediate. Its unique spirocyclic structure makes it valuable for constructing complex molecular frameworks, particularly in the development of pharmaceuticals and agrochemicals. It is often employed in the synthesis of bioactive compounds, where the spiro ring system can contribute to enhanced stability or specific biological activity. Additionally, its ester functional group allows for further chemical modifications, enabling the creation of diverse derivatives for research and industrial applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,310.00
inventory 10g
10-20 days ฿40,640.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
ETHYL 6-OXASPIRO[2.5]OCTANE-1-CARBOXYLATE
No image available

This chemical is primarily utilized in organic synthesis as a versatile intermediate. Its unique spirocyclic structure makes it valuable for constructing complex molecular frameworks, particularly in the development of pharmaceuticals and agrochemicals. It is often employed in the synthesis of bioactive compounds, where the spiro ring system can contribute to enhanced stability or specific biological activity. Additionally, its ester functional group allows for further chemical modifications, enabling th

This chemical is primarily utilized in organic synthesis as a versatile intermediate. Its unique spirocyclic structure makes it valuable for constructing complex molecular frameworks, particularly in the development of pharmaceuticals and agrochemicals. It is often employed in the synthesis of bioactive compounds, where the spiro ring system can contribute to enhanced stability or specific biological activity. Additionally, its ester functional group allows for further chemical modifications, enabling the creation of diverse derivatives for research and industrial applications.

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...