CAS 463-11-6

1-Fluorooctane

Description:

1-Fluorooctane is an organic compound classified as a fluorinated alkane, specifically an octane derivative where one hydrogen atom is replaced by a fluorine atom. Its molecular formula is C8H17F, and it features a straight-chain structure with eight carbon atoms. This compound is typically a colorless liquid at room temperature and possesses a relatively low boiling point compared to non-fluorinated alkanes of similar chain length. 1-Fluorooctane is characterized by its hydrophobic nature, making it insoluble in water but soluble in organic solvents. The presence of the fluorine atom imparts unique properties, such as increased chemical stability and altered reactivity compared to its non-fluorinated counterparts. It is used in various applications, including as a solvent, in chemical synthesis, and in the study of fluorinated compounds' behavior in different environments. Safety considerations are important, as fluorinated compounds can exhibit toxicity and environmental persistence. Proper handling and disposal protocols should be followed to mitigate any potential risks associated with its use.

Formula: C₈H₁₇F

InChI: InChI=1S/C8H17F/c1-2-3-4-5-6-7-8-9/h2-8H2,1H3

InChI key: InChIKey=DHIVLKMGKIZOHF-UHFFFAOYSA-N

SMILES: C(CCCC)CCCF

Synonyms:

• 1-Fluorooctane
• 1-Octyl fluoride
• NSC 62037
• Octane, 1-fluoro-
• n-Octyl fluoride
• Octyl fluoride

1-Fluorooctane

CAS: 463-11-6

Formula: C₈H₁₇F

Purity: 98%

Molecular weight: 132.2190

Ref: IN-DA003ECC

Octyl fluoride

CAS: 463-11-6

Octyl fluoride

Formula: C₈H₁₇F

Purity: 98%

Color and Shape: clear. almost colourless liquid

Molecular weight: 132.22g/mol

Ref: 54-PC5360

1-Fluorooctane

CAS: 463-11-6

Purity: 98%

Molecular weight: 132.22

Ref: 10-F003482

1-Fluorooctane

CAS: 463-11-6

1-Fluorooctane is a chemical compound that is a member of the diphenyl ether family. 1-Fluorooctane has been shown to inhibit choroidal neovascularization in rats by reducing dry weight, serum alanine, and growth factor levels. 1-Fluorooctane also inhibits the production of chloride in vitro. The mechanism of action is unknown, but may be due to its ability to act as an amino transferase inhibitor. This compound has been shown to be effective at inhibiting the activity of protein kinases such as glycogen synthase kinase 3β (GSK3β) and protein tyrosine kinases such as platelet-derived growth factor receptor β (PDGFRβ).

Formula: C₈H₁₇F

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 132.22 g/mol

Ref: 3D-AAA46311