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681260-24-2

3-(3-Chlorophenyl)-1H-pyrazole-4-carbaldehyde

Catalog#: AR00J6BT  |   CAS#: 681260-24-2  |   MDL#: MFCD02656621  |   MF: C10H7ClN2O  |   MW: 206.6284

Packsize Purity Price Availability Quantity
50mg 95% $221.00 2-3 weeks Buy Now Add To Cart
100mg 95% $316.00 2-3 weeks Buy Now Add To Cart
250mg 95% $439.00 2-3 weeks Buy Now Add To Cart
500mg 95% $696.00 2-3 weeks Buy Now Add To Cart
1g 95% $889.00 2-3 weeks Buy Now Add To Cart
2.5g 95% $1,717.00 2-3 weeks Buy Now Add To Cart
5g 95% $2,529.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR00J6BT
Chemical Name 3-(3-Chlorophenyl)-1H-pyrazole-4-carbaldehyde
CAS Number 681260-24-2
Molecular Formula C10H7ClN2O
Molecular Weight 206.6284
MDL Number MFCD02656621
SMILES O=Cc1c[nH]nc1c1cccc(c1)Cl

3-(3-Chlorophenyl)-1H-pyrazole-4-carboxaldehyde is a versatile compound commonly utilized in chemical synthesis for its unique properties and functions. This compound serves as a crucial building block in the creation of various organic molecules due to its structural characteristics and reactivity.Firstly, 3-(3-Chlorophenyl)-1H-pyrazole-4-carboxaldehyde is commonly employed as a key intermediate in the synthesis of pharmaceutical compounds. It can undergo various chemical transformations, such as reduction, oxidation, and functional group interconversion, to yield biologically active molecules with diverse pharmacological activities. This highlights its significance in drug discovery and development processes.Furthermore, this compound is a valuable precursor in the preparation of functionalized heterocyclic compounds. By incorporating 3-(3-Chlorophenyl)-1H-pyrazole-4-carboxaldehyde into synthetic routes, chemists can access a wide range of pyrazole derivatives, which have applications in medicinal chemistry, material science, and agrochemicals.Additionally, 3-(3-Chlorophenyl)-1H-pyrazole-4-carboxaldehyde can be utilized in the synthesis of various organic compounds with specialized properties. Its reactivity allows for the introduction of specific functional groups or modifications, enabling the tailored design of molecules for specific applications in fields like organic electronics, catalysis, and materials science.In conclusion, the versatility and reactivity of 3-(3-Chlorophenyl)-1H-pyrazole-4-carboxaldehyde make it a valuable tool in chemical synthesis, enabling the efficient construction of complex organic molecules with diverse applications in pharmaceuticals, materials, and other scientific disciplines.
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