2,2-Dimethoxycyclohexan-1-one

95%

Reagent Code: #167531
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CAS Number 38461-13-1

science Other reagents with same CAS 38461-13-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.2 g/mol
Formula C₈H₁₄O₃
badge Registry Numbers
MDL Number MFCD24688006
inventory_2 Storage & Handling
Storage -20°C, Inert Gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the pharmaceutical and fine chemical industries. It serves as a building block for the preparation of complex cyclic compounds due to the presence of reactive ketone and acetal functional groups. Its structure allows for selective transformations, making it valuable in the synthesis of bioactive molecules, fragrances, and specialty materials. The compound is also employed in academic research to explore new reaction pathways involving carbonyl and masked carbonyl functionalities.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,310.00
inventory 1g
10-20 days ฿42,670.00
inventory 250mg
10-20 days ฿15,810.00

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2,2-Dimethoxycyclohexan-1-one
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Used as an intermediate in organic synthesis, particularly in the pharmaceutical and fine chemical industries. It serves as a building block for the preparation of complex cyclic compounds due to the presence of reactive ketone and acetal functional groups. Its structure allows for selective transformations, making it valuable in the synthesis of bioactive molecules, fragrances, and specialty materials. The compound is also employed in academic research to explore new reaction pathways involving carbonyl

Used as an intermediate in organic synthesis, particularly in the pharmaceutical and fine chemical industries. It serves as a building block for the preparation of complex cyclic compounds due to the presence of reactive ketone and acetal functional groups. Its structure allows for selective transformations, making it valuable in the synthesis of bioactive molecules, fragrances, and specialty materials. The compound is also employed in academic research to explore new reaction pathways involving carbonyl and masked carbonyl functionalities.

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