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99329-85-8

2-Chloro-4-fluoro-5-nitrobenzaldehyde

Catalog#: AR005TFI  |   CAS#: 99329-85-8  |   MDL#: MFCD17168722  |   MF: C7H3ClFNO3  |   MW: 203.5550

Packsize Purity Price Availability Quantity
100mg 96% $4.00 Global Stock Buy Now Add To Cart
250mg 96% $5.00 Global Stock Buy Now Add To Cart
1g 96% $5.00 Global Stock Buy Now Add To Cart
5g 96% $13.00 Global Stock Buy Now Add To Cart
10g 96% $26.00 Global Stock Buy Now Add To Cart
25g 96% $48.00 Global Stock Buy Now Add To Cart
50g 96% $90.00 Global Stock Buy Now Add To Cart
100g 96% $169.00 Global Stock Buy Now Add To Cart
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Catalog Number AR005TFI
Chemical Name 2-Chloro-4-fluoro-5-nitrobenzaldehyde
CAS Number 99329-85-8
Molecular Formula C7H3ClFNO3
Molecular Weight 203.5550
MDL Number MFCD17168722
SMILES O=Cc1cc([N+](=O)[O-])c(cc1Cl)F

2-Chloro-4-fluoro-5-nitrobenzaldehyde is a versatile compound commonly utilized in chemical synthesis for its unique properties and reactivity. This compound is a key building block in organic chemistry, particularly in the production of pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, 2-Chloro-4-fluoro-5-nitrobenzaldehyde serves as a valuable intermediate for the preparation of various compounds due to its functional groups that enable it to undergo a wide range of reactions. It can be used in the synthesis of heterocyclic compounds, dyes, and other complex organic molecules.The presence of the nitro, chloro, and fluoro substituents on the benzaldehyde ring provides multiple avenues for further functionalization and derivatization. These functional groups can participate in substitution, reduction, and oxidation reactions, allowing for the introduction of different chemical moieties to tailor the properties of the final product.Additionally, the electron-withdrawing nature of the nitro and fluoro groups, along with the electron-donating nature of the chloro group, can influence the reactivity and selectivity of reactions involving 2-Chloro-4-fluoro-5-nitrobenzaldehyde, making it a valuable tool for synthetic chemists seeking to control regioselectivity and stereoselectivity in their reactions.Overall, the application of 2-Chloro-4-fluoro-5-nitrobenzaldehyde in chemical synthesis is vital for the creation of diverse chemical compounds with specific structures and properties, making it a crucial component in the toolkit of synthetic chemists across various industries.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class -
Packing Group -

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