4-Chloro-2-methoxyphenol

98%

Reagent Code: #159420
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CAS Number 16766-30-6

science Other reagents with same CAS 16766-30-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.58 g/mol
Formula C₇H₇ClO₂
badge Registry Numbers
MDL Number MFCD00070774
thermostat Physical Properties
Boiling Point 242.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, Inert gas storage

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of herbicides and fungicides. It serves as a building block in organic reactions due to the presence of reactive functional groups—phenolic hydroxyl and chloro substituent—enabling coupling and substitution reactions. Also employed in the development of flavor and fragrance compounds, where its aromatic structure contributes to smoky or spicy sensory notes. Its methoxy and chloro groups enhance stability and influence lipophilicity, making it suitable for use in certain biologically active molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿420.00
5g
10-20 days ฿2,010.00
4-Chloro-2-methoxyphenol
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of herbicides and fungicides. It serves as a building block in organic reactions due to the presence of reactive functional groups—phenolic hydroxyl and chloro substituent—enabling coupling and substitution reactions. Also employed in the development of flavor and fragrance compounds, where its aromatic structure contributes to smoky or spicy sensory notes. Its methoxy and chloro groups enhance s

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of herbicides and fungicides. It serves as a building block in organic reactions due to the presence of reactive functional groups—phenolic hydroxyl and chloro substituent—enabling coupling and substitution reactions. Also employed in the development of flavor and fragrance compounds, where its aromatic structure contributes to smoky or spicy sensory notes. Its methoxy and chloro groups enhance stability and influence lipophilicity, making it suitable for use in certain biologically active molecules.

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