3-Chloro-4,5-dimethoxybenzaldehyde

95%

Reagent Code: #162663
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CAS Number 18268-68-3

science Other reagents with same CAS 18268-68-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.619 g/mol
Formula C₉H₉ClO₃
badge Registry Numbers
MDL Number MFCD02256335
thermostat Physical Properties
Melting Point 56 - 60 ℃
Boiling Point 301.8 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.245 g/cm3
Storage -20 °C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of certain central nervous system agents and psychoactive drugs. It plays a role in the preparation of substituted amphetamines and related compounds due to its aldehyde functional group and methoxy substitution pattern, which allow for selective chemical modifications. Also utilized in research settings for the development of novel organic compounds and in the creation of analogs for structure-activity relationship studies. Its reactivity makes it valuable in forming carbon-carbon bonds through condensation and nucleophilic addition reactions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,030.00
inventory 250mg
10-20 days ฿1,570.00

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3-Chloro-4,5-dimethoxybenzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of certain central nervous system agents and psychoactive drugs. It plays a role in the preparation of substituted amphetamines and related compounds due to its aldehyde functional group and methoxy substitution pattern, which allow for selective chemical modifications. Also utilized in research settings for the development of novel organic compounds and in the creation of analogs for structure-activity relatio

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of certain central nervous system agents and psychoactive drugs. It plays a role in the preparation of substituted amphetamines and related compounds due to its aldehyde functional group and methoxy substitution pattern, which allow for selective chemical modifications. Also utilized in research settings for the development of novel organic compounds and in the creation of analogs for structure-activity relationship studies. Its reactivity makes it valuable in forming carbon-carbon bonds through condensation and nucleophilic addition reactions.

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