73448-14-3 | 5-Hexynoic acid tert-butyl ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$73.00	$52.00
1g	98%	in stock	$209.00	$147.00

Description

• Catalog Number: AB53649
• Chemical Name: 5-Hexynoic acid tert-butyl ester
• CAS Number: 73448-14-3
• Molecular Formula: C10H16O2
• Molecular Weight: 168.2328
• MDL Number: MFCD13192076
• SMILES: C#CCCCC(=O)OC(C)(C)C

Computed Properties

• Complexity: 190
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• XLogP3: 2

Upstream Synthesis Route

5-Hexynoic acid tert-butyl ester is a versatile compound frequently utilized in chemical synthesis due to its unique properties and reactivity. This ester serves as a valuable building block in the creation of various organic molecules, thanks to its ability to participate in a range of chemical reactions.One common application of 5-Hexynoic acid tert-butyl ester is in the formation of new carbon-carbon bonds through cross-coupling reactions. By coupling this ester with suitable partners, such as organometallic reagents, researchers can efficiently construct complex organic structures with high precision.Additionally, the alkyne functionality present in 5-Hexynoic acid tert-butyl ester enables it to undergo various transformations, including cycloaddition reactions and metal-catalyzed processes. This versatility opens up avenues for the synthesis of diverse organic compounds, making it a valuable tool in the toolbox of synthetic chemists.Moreover, the tert-butyl ester moiety in this compound provides protection for the carboxylic acid group, allowing for selective manipulation of the molecule's other functional groups. This protection-deprotection strategy is crucial in multi-step synthesis, where control over reactivity is essential for the successful formation of the desired products.In conclusion, the application of 5-Hexynoic acid tert-butyl ester in chemical synthesis encompasses its role as a key intermediate in building complex organic molecules, its participation in diverse chemical transformations, and its utility in selective functional group manipulations. This compound's versatility and reactivity make it a valuable asset for researchers engaged in the creation of novel materials and pharmaceuticals.