178312-47-5 | Ethyl 4,4-difluorocyclohexanecarboxylate

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$18.00	$12.00
5g	97%	in stock	$22.00	$16.00
100g	97%	in stock	$417.00	$292.00
500g	97%	in stock	$1,862.00	$1,304.00

Description

• Catalog Number: AB00787
• Chemical Name: Ethyl 4,4-difluorocyclohexanecarboxylate
• CAS Number: 178312-47-5
• Molecular Formula: C9H14F2O2
• Molecular Weight: 192.2031
• MDL Number: MFCD03788494
• SMILES: CCOC(=O)C1CCC(CC1)(F)F

Computed Properties

• Complexity: 182
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• XLogP3: 2.3

Upstream Synthesis Route

Ethyl 4,4-Difluorocyclohexanecarboxylate is a valuable compound widely utilized in chemical synthesis due to its unique properties and versatile applications. This compound serves as a key building block in the creation of various organic molecules, particularly in the pharmaceutical and agrochemical industries.In chemical synthesis, Ethyl 4,4-Difluorocyclohexanecarboxylate acts as a precursor for the production of complex molecules through strategic functional group transformations. Its difluoromethyl group provides a valuable source of fluorine atoms, enhancing the properties of resulting compounds such as increased metabolic stability and improved bioavailability in drug molecules.Furthermore, Ethyl 4,4-Difluorocyclohexanecarboxylate enables chemists to introduce specific structural motifs into target molecules, leading to the development of novel pharmaceuticals, crop protection agents, and materials with enhanced properties. Its strategic incorporation can alter the pharmacokinetic profile, biological activity, or physical characteristics of the final products, making it a versatile tool in organic synthesis.Overall, Ethyl 4,4-Difluorocyclohexanecarboxylate plays a crucial role in the design and synthesis of advanced chemical compounds with diverse applications, highlighting its significance in the field of modern chemistry.

Literature

• Aminodifluorosulfinium salts: selective fluorination reagents with enhanced thermal stability and ease of handling.

  The Journal of organic chemistry 20100521