3-Chloro-5-formylbenzonitrile

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Reagent Code: #65524
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CAS Number 1205513-88-7

science Other reagents with same CAS 1205513-88-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.58 g/mol
Formula C₈H₄ClNO
badge Registry Numbers
MDL Number MFCD18392412
thermostat Physical Properties
Boiling Point 225.5±20.0 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.32±0.1 g/cm3
Storage room temperature

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its reactive formyl and nitrile groups make it valuable for constructing complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). Additionally, it is employed in the synthesis of dyes and pigments due to its ability to form stable aromatic structures. In research, it is utilized for studying reaction mechanisms and developing novel chemical processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,710.00
inventory 1g
10-20 days ฿2,925.00
inventory 5g
10-20 days ฿8,865.00

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3-Chloro-5-formylbenzonitrile
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its reactive formyl and nitrile groups make it valuable for constructing complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). Additionally, it is employed in the synthesis of dyes and pigments due to its ability to form stable aromatic structures. In research, it is utilized for studying reaction mechanisms and developin

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its reactive formyl and nitrile groups make it valuable for constructing complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). Additionally, it is employed in the synthesis of dyes and pigments due to its ability to form stable aromatic structures. In research, it is utilized for studying reaction mechanisms and developing novel chemical processes.

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