2-(3-Chloropropyl)-2-(4-fluorophenyl)-1,3-dioxolane

≥95%

Reagent Code: #156995
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CAS Number 3308-94-9

science Other reagents with same CAS 3308-94-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.69 g/mol
Formula C₁₂H₁₄ClFO₂
badge Registry Numbers
MDL Number MFCD00020909
thermostat Physical Properties
Boiling Point 112°C/0.01mmHg(lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of reactive functional groups. Commonly employed in research settings for designing analogs of neuroactive drugs. Also utilized in the preparation of fluorinated organic compounds to enhance metabolic stability and binding affinity in drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿540.00
1g
10-20 days ฿1,830.00
5g
10-20 days ฿7,180.00
25g
10-20 days ฿28,760.00

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2-(3-Chloropropyl)-2-(4-fluorophenyl)-1,3-dioxolane
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of reactive functional groups. Commonly employed in research settings for designing analogs of neuroactive drugs. Also utilized in the preparation of fluorinated organic compounds to enhance metabolic stability and binding affinity in drug candidates.

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of reactive functional groups. Commonly employed in research settings for designing analogs of neuroactive drugs. Also utilized in the preparation of fluorinated organic compounds to enhance metabolic stability and binding affinity in drug candidates.

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