1227499-98-0 | 3-Fluoro-5-(trifluoromethyl)picolinaldehyde

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$124.00	$87.00
250mg	97%	in stock	$210.00	$147.00
500mg	97%	in stock	$315.00	$221.00
1g	97%	in stock	$526.00	$369.00
5g	97%	in stock	$1,842.00	$1,290.00

Description

• Catalog Number: AA24785
• Chemical Name: 3-Fluoro-5-(trifluoromethyl)picolinaldehyde
• CAS Number: 1227499-98-0
• Molecular Formula: C7H3F4NO
• Molecular Weight: 193.0984
• MDL Number: MFCD16606940
• SMILES: O=Cc1ncc(cc1F)C(F)(F)F

Computed Properties

• Complexity: 193
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1
• XLogP3: 1.6

Upstream Synthesis Route

3-Fluoro-5-(trifluoromethyl)picolinaldehyde is a versatile compound widely employed in chemical synthesis for its unique reactivity and structural features. This aldehyde derivative is particularly valuable in organic synthesis due to its ability to act as a key building block in the preparation of various functionalized molecules.Firstly, 3-Fluoro-5-(trifluoromethyl)picolinaldehyde is utilized in the synthesis of pharmaceutical intermediates and agrochemicals. Its structural characteristics make it a valuable precursor in the development of bioactive compounds, serving as a crucial starting material in the construction of complex molecular architectures.Additionally, this compound finds application in the field of materials science, where it is employed in the preparation of novel materials with tailored properties. By incorporating 3-Fluoro-5-(trifluoromethyl)picolinaldehyde into various polymeric systems and coordination complexes, researchers can access materials with desirable characteristics such as enhanced stability, reactivity, or optical properties.Furthermore, the reactivity of 3-Fluoro-5-(trifluoromethyl)picolinaldehyde allows for its use in the development of fluorescent probes and dyes. Chemists exploit its unique structural motifs to design molecular probes capable of selectively interacting with specific biological targets or reporting on chemical processes in real-time, enabling advancements in bioimaging and sensor technologies.