CAS 134364-69-5

1,2-Difluoro-3-methoxybenzene

Description:

1,2-Difluoro-3-methoxybenzene, also known by its CAS number 134364-69-5, is an aromatic compound characterized by the presence of two fluorine atoms and a methoxy group (-OCH3) attached to a benzene ring. The fluorine substituents are located at the 1 and 2 positions, while the methoxy group is positioned at the 3 position, resulting in a specific molecular geometry that influences its chemical properties. This compound is typically a colorless to pale yellow liquid with a distinctive aromatic odor. It is known for its moderate polarity due to the electronegative fluorine atoms, which can enhance its reactivity in various chemical reactions, including nucleophilic substitutions. Additionally, the methoxy group can participate in hydrogen bonding, affecting solubility in polar solvents. 1,2-Difluoro-3-methoxybenzene is utilized in organic synthesis and may serve as an intermediate in the production of pharmaceuticals and agrochemicals. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.

Formula: C₇H₆F₂O

InChI: InChI=1S/C7H6F2O/c1-10-6-4-2-3-5(8)7(6)9/h2-4H,1H3

InChI key: InChIKey=RDOGTTNFVLSBKG-UHFFFAOYSA-N

SMILES: O(C)C1=C(F)C(F)=CC=C1

Synonyms:

• 1,1,1-Trifluoro-2-Phenylbut-3-En-2-Ol
• 1,2-Difluoro-3-Methoxybenzene
• 1-Methoxy-2,3-Difluorobenzene
• 2,3-Difluorophenyl methyl ether
• Benzene, 1,2-difluoro-3-methoxy-
• Difluoroanisole1
• 2,3-Difluoroanisole

2,3-Difluoroanisole

CAS: 134364-69-5

Formula: C₇H₆F₂O

Purity: 98%

Color and Shape: Liquid

Molecular weight: 144.1187

Ref: IN-DA003FII

2,3-Difluoroanisole

CAS: 134364-69-5

2,3-Difluoroanisole

Formula: C₇H₆F₂O

Purity: ≥95%

Color and Shape: Liquid

Molecular weight: 144.11874g/mol

Ref: 54-PC0218

2,3-Difluoroanisole

CAS: 134364-69-5

2,3-Difluoroanisole is a synthetic organic compound that is used in the preparation of other organic compounds. It is prepared by the amination reaction of chloroacetic acid and 2,3-difluoroethanol. The anticancer activity of 2,3-difluoroanisole has been studied extensively. This compound inhibits the growth of cancer cells by inhibiting DNA synthesis and protein synthesis. The inhibitory effects are due to the chlorine atom on the molecule, which can react with hydrogen atoms on amino groups on enzymes, thereby preventing these enzymes from functioning properly. 2,3-Difluoroanisole also has inhibitory properties against olefinic reactions such as formylation or chemists reactions at high temperatures.

Formula: C₇H₆F₂O

Purity: Min. 95%

Molecular weight: 144.12 g/mol

Ref: 3D-FD70438

2,3-Difluoroanisole

CAS: 134364-69-5

Formula: C₇H₆F₂O

Purity: 98%

Color and Shape: Liquid

Molecular weight: 144.121

Ref: 10-F005734

2,3-Difluoroanisole

CAS: 134364-69-5

Formula: C₇H₆F₂O

Purity: >97.0%(GC)

Color and Shape: Colorless to Almost colorless clear liquid

Molecular weight: 144.12

Ref: 3B-D3359