BENZO[1,3]DIOXOL-5-YL-ACETYL CHLORIDE

≥95%

Reagent Code: #141704
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CAS Number 6845-81-4

science Other reagents with same CAS 6845-81-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.6031 g/mol
Formula C₉H₇ClO₃
badge Registry Numbers
MDL Number MFCD03424722
thermostat Physical Properties
Melting Point 129-131 °C
Boiling Point 110-112 °C
inventory_2 Storage & Handling
Density 1.399±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals and fine chemicals. Its reactive acyl chloride group allows for easy formation of amide and ester derivatives, making it valuable in drug development. Commonly employed in the preparation of psychoactive compounds and research chemicals, particularly those related to substituted phenethylamines and amphetamines. Also utilized in organic synthesis for introducing the benzo[1,3]dioxol-5-yl acetyl moiety into larger molecules, enhancing structural complexity for biological activity studies. Handle with care due to its moisture sensitivity and potential lachrymatory effects.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,200.00
inventory 250mg
10-20 days ฿4,800.00

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BENZO[1,3]DIOXOL-5-YL-ACETYL CHLORIDE
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Used primarily as a key intermediate in the synthesis of pharmaceuticals and fine chemicals. Its reactive acyl chloride group allows for easy formation of amide and ester derivatives, making it valuable in drug development. Commonly employed in the preparation of psychoactive compounds and research chemicals, particularly those related to substituted phenethylamines and amphetamines. Also utilized in organic synthesis for introducing the benzo[1,3]dioxol-5-yl acetyl moiety into larger molecules, enhancin

Used primarily as a key intermediate in the synthesis of pharmaceuticals and fine chemicals. Its reactive acyl chloride group allows for easy formation of amide and ester derivatives, making it valuable in drug development. Commonly employed in the preparation of psychoactive compounds and research chemicals, particularly those related to substituted phenethylamines and amphetamines. Also utilized in organic synthesis for introducing the benzo[1,3]dioxol-5-yl acetyl moiety into larger molecules, enhancing structural complexity for biological activity studies. Handle with care due to its moisture sensitivity and potential lachrymatory effects.

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