1,2-Benzenediol, 4,5-difluoro- (9CI), with the CAS number 147300-08-1, is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with two hydroxyl (–OH) groups and two fluorine atoms. The presence of the hydroxyl groups indicates that it is a diol, which can participate in hydrogen bonding, potentially affecting its solubility and reactivity. The fluorine substituents enhance the compound's polarity and can influence its chemical behavior, including reactivity and interaction with biological systems. This compound may exhibit unique properties such as altered boiling and melting points compared to its non-fluorinated counterparts. Additionally, the specific arrangement of the substituents on the benzene ring can lead to distinct stereochemical properties, impacting its applications in various fields, including pharmaceuticals and materials science. Overall, 1,2-Benzenediol, 4,5-difluoro- is a compound of interest due to its potential utility in synthetic chemistry and its unique physical and chemical properties.

1,2-Benzenediol,4,5-difluoro-(9CI)

147300-08-1: 1,2-Benzenediol, 4,5-difluoro-, 4,5-Difluoro-1,2-benzenediol, 4,5-Difluoro-2-hydroxyphenol, 4,5-Difluorobenzene-1,2-diol, 4,5-Difluorocatechol, Benzene-1,2-diol, 4,5-difluoro-

4,5-Difluorobenzene-1,2-diol

1,2-Benzenediol, 4,5-difluoro-

4,5-Difluorobenzene-1,2-diol is a molecule that has an energy barrier due to the steric hindrance of the catecholate substituents. The inactivation process is irreversible and it can be substituted with nucleophiles. 4,5-Difluorobenzene-1,2-diol is reactive because it has an orbital that can react with electrophiles. The reaction mechanism for this compound is nucleophilic substitution at the carbonyl carbon.

CAS 147300-08-1: 1,2-Benzenediol,4,5-difluoro-(9CI)

4,5-Difluorobenzene-1,2-diol

Ref: 54-PC9889

1,2-Benzenediol, 4,5-difluoro-

Ref: IN-DA001ES0

4,5-Difluorobenzene-1,2-diol

Ref: 10-F238372

4,5-Difluorobenzene-1,2-diol

Ref: 3D-FD78953