2-(2-Chloropyridin-4-yl)acetic acid

97%

Reagent Code: #162667
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CAS Number 887580-55-4

science Other reagents with same CAS 887580-55-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.58 g/mol
Formula C₇H₆ClNO₂
badge Registry Numbers
MDL Number MFCD07367936
thermostat Physical Properties
Melting Point 140 - 145 ℃
Boiling Point 338.8 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.405 g/cm3
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of neonicotinoid insecticides, particularly in the production of imidacloprid and related compounds. It plays a critical role in forming the chloropyridyl moiety that contributes to the insecticidal activity. The compound is also utilized in agrochemical research for developing new crop protection agents due to its reactivity and structural properties. Its derivatives show systemic action in plants, making them effective against sap-feeding insects like aphids and whiteflies.

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Test Parameter Specification
Appearance White to Off-White Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,300.00
inventory 1g
10-20 days ฿2,650.00
inventory 5g
10-20 days ฿12,060.00
inventory 100mg
10-20 days ฿1,000.00

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2-(2-Chloropyridin-4-yl)acetic acid
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Used as a key intermediate in the synthesis of neonicotinoid insecticides, particularly in the production of imidacloprid and related compounds. It plays a critical role in forming the chloropyridyl moiety that contributes to the insecticidal activity. The compound is also utilized in agrochemical research for developing new crop protection agents due to its reactivity and structural properties. Its derivatives show systemic action in plants, making them effective against sap-feeding insects like aphids and
Used as a key intermediate in the synthesis of neonicotinoid insecticides, particularly in the production of imidacloprid and related compounds. It plays a critical role in forming the chloropyridyl moiety that contributes to the insecticidal activity. The compound is also utilized in agrochemical research for developing new crop protection agents due to its reactivity and structural properties. Its derivatives show systemic action in plants, making them effective against sap-feeding insects like aphids and whiteflies.
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