2-Chloro-3-methylbenzaldehyde

95%

Reagent Code: #162225
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CAS Number 61563-28-8

science Other reagents with same CAS 61563-28-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.59 g/mol
Formula C₈H₇ClO
badge Registry Numbers
MDL Number MFCD11845907
thermostat Physical Properties
Boiling Point 228.394°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) for anti-inflammatory and analgesic drugs. It serves as a building block in organic reactions, especially in the development of agrochemicals such as herbicides and fungicides. Its structure allows for functionalization in multi-step syntheses, making it valuable in the preparation of dyes, fragrances, and specialty chemicals. Commonly employed in condensation reactions to form carbon-carbon bonds, it contributes to the creation of more complex aromatic compounds used in research and industrial applications.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Colorless to brown 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 100mg
10-20 days ฿220.00
inventory 250mg
10-20 days ฿412.50
inventory 5g
10-20 days ฿9,770.00
inventory 10g
10-20 days ฿16,740.00
inventory 1g
10-20 days ฿2,420.00

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2-Chloro-3-methylbenzaldehyde
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) for anti-inflammatory and analgesic drugs. It serves as a building block in organic reactions, especially in the development of agrochemicals such as herbicides and fungicides. Its structure allows for functionalization in multi-step syntheses, making it valuable in the preparation of dyes, fragrances, and specialty chemicals. Commonly employed in condensation reactions to form carbon-carbon bonds, it contributes to the creation of more complex aromatic compounds used in research and industrial applications.
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