3-Cyanobenzoyl chloride

95%

Reagent Code: #162014
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CAS Number 1711-11-1

science Other reagents with same CAS 1711-11-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.58 g/mol
Formula C₈H₄ClNO
badge Registry Numbers
MDL Number MFCD00011545
thermostat Physical Properties
Boiling Point 125-129°C at 11 mmHg
inventory_2 Storage & Handling
Density 1.32g/cm3
Storage 2-8°C, stored in inert gas

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It serves as a building block for the preparation of various heterocyclic compounds due to the reactivity of both the acyl chloride and nitrile functional groups. The acyl chloride group readily reacts with amines and alcohols to form amides and esters, respectively, enabling the construction of complex molecules. Its nitrile group can be hydrolyzed to carboxylic acids or reduced to amines, offering further derivatization pathways. Commonly employed in the synthesis of active pharmaceutical ingredients (APIs), particularly in compounds targeting central nervous system disorders and anti-inflammatory agents. Also utilized in the development of crop protection chemicals, where its structure contributes to the biological activity of certain herbicides and fungicides.

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Test Parameter Specification
Appearance White to yellow to light brown Crystals or crystalline mass and/or chunks
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,330.00
inventory 10g
10-20 days ฿15,000.00
inventory 5g
10-20 days ฿8,330.00

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3-Cyanobenzoyl chloride
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It serves as a building block for the preparation of various heterocyclic compounds due to the reactivity of both the acyl chloride and nitrile functional groups. The acyl chloride group readily reacts with amines and alcohols to form amides and esters, respectively, enabling the construction of complex molecules. Its nitrile group can be hydrolyzed to carboxylic acids or reduced to amine

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It serves as a building block for the preparation of various heterocyclic compounds due to the reactivity of both the acyl chloride and nitrile functional groups. The acyl chloride group readily reacts with amines and alcohols to form amides and esters, respectively, enabling the construction of complex molecules. Its nitrile group can be hydrolyzed to carboxylic acids or reduced to amines, offering further derivatization pathways. Commonly employed in the synthesis of active pharmaceutical ingredients (APIs), particularly in compounds targeting central nervous system disorders and anti-inflammatory agents. Also utilized in the development of crop protection chemicals, where its structure contributes to the biological activity of certain herbicides and fungicides.

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