4,4-Dimethylcyclohexanone

98%

Reagent Code: #169729
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CAS Number 4255-62-3

science Other reagents with same CAS 4255-62-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 126.2 g/mol
Formula C₈H₁₄O
badge Registry Numbers
MDL Number MFCD00234965
thermostat Physical Properties
Melting Point 41-45 °C
Boiling Point 105-106℃ (80 Torr)
inventory_2 Storage & Handling
Density 0.892±0.06 g/cm3 (20 ºC 760 Torr)
Storage Room temperature

description Product Description

Used in the synthesis of fragrances and flavoring agents due to its stable ketone structure that can undergo selective reactions. Serves as an intermediate in the production of pharmaceuticals, particularly in the development of steroid analogs and anti-inflammatory compounds. Employed in organic synthesis for creating substituted cyclohexanes, which are important building blocks in agrochemicals and specialty polymers. Its symmetrical structure and steric hindrance make it suitable for studying reaction mechanisms involving nucleophilic addition and reduction under controlled conditions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿156.00
inventory 1g
10-20 days ฿180.00
inventory 5g
10-20 days ฿750.00
inventory 25g
10-20 days ฿3,330.00
inventory 100g
10-20 days ฿9,480.00
inventory 500g
10-20 days ฿47,380.00

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4,4-Dimethylcyclohexanone
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Used in the synthesis of fragrances and flavoring agents due to its stable ketone structure that can undergo selective reactions. Serves as an intermediate in the production of pharmaceuticals, particularly in the development of steroid analogs and anti-inflammatory compounds. Employed in organic synthesis for creating substituted cyclohexanes, which are important building blocks in agrochemicals and specialty polymers. Its symmetrical structure and steric hindrance make it suitable for studying reaction

Used in the synthesis of fragrances and flavoring agents due to its stable ketone structure that can undergo selective reactions. Serves as an intermediate in the production of pharmaceuticals, particularly in the development of steroid analogs and anti-inflammatory compounds. Employed in organic synthesis for creating substituted cyclohexanes, which are important building blocks in agrochemicals and specialty polymers. Its symmetrical structure and steric hindrance make it suitable for studying reaction mechanisms involving nucleophilic addition and reduction under controlled conditions.

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