CAS 53412-38-7

2H-1,4-Benzoxazin-3(4H)-one,6-hydroxy-

Description:

2H-1,4-Benzoxazin-3(4H)-one, 6-hydroxy- (CAS 53412-38-7) is a chemical compound characterized by its heterocyclic structure, which includes a benzene ring fused to a benzoxazine moiety. This compound features a hydroxyl group at the 6-position, contributing to its potential reactivity and solubility in polar solvents. It is known for its role in various biological activities, including potential antioxidant properties and applications in agricultural chemistry as a natural defense mechanism in plants. The presence of the hydroxyl group enhances its ability to participate in hydrogen bonding, influencing its physical properties such as melting point and solubility. Additionally, compounds of this class may exhibit fluorescence, making them of interest in materials science and organic synthesis. Overall, 2H-1,4-Benzoxazin-3(4H)-one, 6-hydroxy- is a versatile compound with implications in both biological and chemical research.

Formula: C₈H₇NO₃

Synonyms:

• 6-Hydroxy-2H-1,4-benzoxazin-3(4H)-one
• 6-Hydroxy-3,4-dihydro-2H-1,4-benzoxazin-3-one
• 6-Hydroxy-3-oxo-3,4-dihydro-2H-1,4-benzoxazine
• 6-Hydroxy-4H-benzo[1,4]oxazin-3-one
• 6-hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one

6-Hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one

CAS: 53412-38-7

Formula: C₈H₇NO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 165.1461

Ref: IN-DA00DG23

6-Hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one

CAS: 53412-38-7

Formula: C₈H₇NO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 165.148

Ref: 10-F455086

6-Hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one

CAS: 53412-38-7

6-Hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one is a dermatological active substance that is used in the treatment of skin diseases. It has been shown to be an immunosuppressant in animals and humans and can also be used in the treatment of respiratory disease. It has vasotropic properties and is an antiinflammatory agent. 6-Hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one is a topoisomerase II inhibitor that binds to DNA and prevents the unwinding of DNA strands by inhibiting the formation of topoisomerases II–DNA complexes. The compound binds to the C1 position on the cyclohexane ring, which contains both unsubstituted alkyl and unsubstituted aryl groups as well as elements such as silver halide.

Formula: C₈H₇NO₃

Purity: Min. 95%

Molecular weight: 165.15 g/mol

Ref: 3D-DCA41238