2-Chlorocyclopentanone

95%, containing K2CO3 stabilizer

Reagent Code: #159093
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Alias 2-Chlorocyclopentanone
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CAS Number 694-28-0

science Other reagents with same CAS 694-28-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 118.56 g/mol
Formula ClC₅H₇(=O)
badge Registry Numbers
EC Number 211-769-9
MDL Number MFCD00001410
thermostat Physical Properties
Boiling Point 72-74 °C12 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.185 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing cyclopentane-based ring systems. It is commonly employed in the preparation of active pharmaceutical ingredients (APIs), including agents with central nervous system activity. Its reactivity allows for carbon-carbon bond formation, enabling the introduction of functional groups at specific positions on the ring. Also utilized in the synthesis of agrochemicals and specialty chemicals where a substituted cyclopentanone scaffold is required. The presence of both a chlorine and a ketone functional group makes it suitable for sequential transformations in multi-step synthetic routes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿780.00
inventory 5g
10-20 days ฿2,560.00
inventory 25g
10-20 days ฿9,680.00
2-Chlorocyclopentanone
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Used as a key intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing cyclopentane-based ring systems. It is commonly employed in the preparation of active pharmaceutical ingredients (APIs), including agents with central nervous system activity. Its reactivity allows for carbon-carbon bond formation, enabling the introduction of functional groups at specific positions on the ring. Also utilized in the synthesis of agrochemicals and specialty chemicals where a subst

Used as a key intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing cyclopentane-based ring systems. It is commonly employed in the preparation of active pharmaceutical ingredients (APIs), including agents with central nervous system activity. Its reactivity allows for carbon-carbon bond formation, enabling the introduction of functional groups at specific positions on the ring. Also utilized in the synthesis of agrochemicals and specialty chemicals where a substituted cyclopentanone scaffold is required. The presence of both a chlorine and a ketone functional group makes it suitable for sequential transformations in multi-step synthetic routes.

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