2-Chlorocyclohexanol

95%

Reagent Code: #161214
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CAS Number 1561-86-0

science Other reagents with same CAS 1561-86-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 134.6 g/mol
Formula C₆H₁₁ClO
badge Registry Numbers
MDL Number MFCD00003860
thermostat Physical Properties
Melting Point 23°C(凝固点)
Boiling Point 84°C/18mmHg(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a building block for cyclohexane derivatives, enabling the development of complex molecules through substitution and elimination reactions. Its chloro and hydroxyl functional groups allow for selective transformations, making it valuable in research and industrial settings for creating active ingredients in crop protection agents and medicinal compounds.

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Test Parameter Specification
Appearance Colorless to light yellow liquid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿350.00
inventory 5g
10-20 days ฿1,310.00
inventory 25g
10-20 days ฿5,790.00
inventory 100g
10-20 days ฿20,890.00

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2-Chlorocyclohexanol
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Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a building block for cyclohexane derivatives, enabling the development of complex molecules through substitution and elimination reactions. Its chloro and hydroxyl functional groups allow for selective transformations, making it valuable in research and industrial settings for creating active ingredients in crop protection agents and medicinal compounds.

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a building block for cyclohexane derivatives, enabling the development of complex molecules through substitution and elimination reactions. Its chloro and hydroxyl functional groups allow for selective transformations, making it valuable in research and industrial settings for creating active ingredients in crop protection agents and medicinal compounds.

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