a-Bromo-γ-butyrolactone

CAS: 5061-21-2

Ref. TR-B682070

Produktinformation

• Name: a-Bromo-γ-butyrolactone
• Synonyme: 3-bromooxolan-2-one, (3R)-3-bromodihydrofuran-2(3H)-one, (3S)-3-bromodihydrofuran-2(3H)-one, 2(3H)-Furanone, 3-bromodihydro-, 2-Bromo-4-Butanolide, 2-Bromo-4-butyrolactone, 2-Bromo-4-hydroxybutyric acid g-lactone, 2-Bromo-4-hydroxybutyric acid gamma-lactone, 2-Bromo-gamma-butyrolactone, 2-Bromo-γ-butyrolactone, 3-Bromo-2-oxotetrahydrofuran, 3-Bromo-4,5-dihydro-2(3H)-furanone, 3-Bromodihydro-2(3H)-furanone, 3-Bromooxolan-2-one, 3-Bromotetrahydrofuran-2-one, 3-bromodihydrofuran-2(3H)-one, Butyric acid, 2-bromo-4-hydroxy-, γ-lactone, Butyric acid, α-bromo-γ-hydroxy-, γ-lactone, NSC 11726, NSC 56959, a-Bromo-γ-butyrolatone, alfa-Bromo-gamma butyrolatone, Α-Bromo-R-Butyrolactone, α-Bromo-γ-butyrolactone, α-Bromobutyric acid γ-lactone
• CAS: 5061-21-2

Beschreibung

Applications Lactams inhibit type Q arylesterase activity of human serum paraoxonase PON1.
References Aldridge, W., et al.: Biochem. J., 53, 110 (1953), Antikainen, M., et al.: J. Clin. Invest., 98, 883 (1996), Aviram, M., et al.: J. Clin. Invest., 101, 1581 (1998), Biggadike, K., et al.: J. Med. Chem., 43, 19 (2000),

• Marke: TRC

Chemische Eigenschaften

• Molekulargewicht: 164.99
• Formel: C₄H₅BrO₂
• Farbe/Form: Neat
• InChl: InChI=1S/C4H5BrO2/c5-3-1-2-7-4(3)6/h3H,1-2H2
• InChI Key: InChIKey=LFJJGHGXHXXDFT-UHFFFAOYSA-N
• SMILES: O=C1OCCC1Br