2-Furancarboxaldehyde, 5-[2-chloro-5-(trifluoromethyl)phenyl]-


Chemical Name: 2-Furancarboxaldehyde, 5-[2-chloro-5-(trifluoromethyl)phenyl]-
CAS Number: 259196-40-2
Product Number: AG002R0X(AGN-PC-0JTZ1O)
Synonyms:
MDL No:
Molecular Formula: C12H6ClF3O2
Molecular Weight: 274.6230

Identification/Properties


Properties
MP:
59-63 °C(lit.);
BP:
336.5°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



5-(2-Chloro-5-(trifluoromethyl)phenyl)furan-2-carbaldehyde plays a crucial role in chemical synthesis as a versatile building block in organic chemistry. This compound serves as a valuable intermediate for the synthesis of various complex molecules in the pharmaceutical, agrochemical, and materials science industries. Its unique structure and functional groups make it a valuable starting material for the creation of diverse organic compounds with desired properties.In chemical synthesis, 5-(2-Chloro-5-(trifluoromethyl)phenyl)furan-2-carbaldehyde can be used as a key reactant in the formation of structurally intricate molecules through a series of well-defined chemical transformations. Its presence in a reaction mixture can facilitate the introduction of specific functional groups, enable the construction of heterocyclic frameworks, and promote the development of novel chemical entities with potential applications in drug discovery and material design.Moreover, the substitution pattern and electronic properties of this compound make it a valuable tool for exploring new synthetic pathways and developing innovative strategies for accessing complex molecular architectures. By leveraging the reactivity of 5-(2-Chloro-5-(trifluoromethyl)phenyl)furan-2-carbaldehyde, chemists can orchestrate a variety of chemical reactions, such as nucleophilic additions, cross-coupling reactions, and multicomponent reactions, to assemble intricate molecules with defined stereochemistry and functionality.