N-(Bromomethyl)phthalimide

CAS: 5332-26-3

Ref. 3D-FB75353

Produktinformation

• Name: N-(Bromomethyl)phthalimide
• Synonyme: 1H-Isoindole-1,3(2H)-dione, 2-(bromomethyl)-, 2-(Bromomethyl)-1H-Isoindole-3(2H)-Dione, 2-(Bromomethyl)-1H-isoindole-1,3(2H)-dione, 2-(Bromomethyl)-2,3-dihydro-1H-isoindole-1,3-dione, 2-(Bromomethyl)isoindoline-1,3-dione, 2-(Bromomethyl)phthalimide, 2-Bromomethylisoindole-1,3-dione, 3a-(bromomethyl)-3a,7a-dihydro-1H-isoindole-1,3(2H)-dione, Bromomethylphthalimide, N-(Bromomethyl)Phtalimide, N-(Bromomethyl)phthalimide,98+%, N-Phthalimidomethyl Bromide, NSC 3997, Phthalimide, N-(bromomethyl)-, Phthalimidomethyl Bromide
• CAS: 5332-26-3

Beschreibung

N-(Bromomethyl)phthalimide is an ethylene acetal that is used for the alkylation of primary and secondary amines. It is a functional group with a thermodynamic stability of -4.5 kcal/mol, which is very close to that of water (-4.8 kcal/mol). This compound has been shown to reduce intraocular pressure in rats by inhibiting the production of aqueous humor and regulating the production of aqueous humor. N-(Bromomethyl)phthalimide also interacts with immunoassay methods, such as immunosorbent assays and ELISA, which are used to detect antibodies or antigens in biological fluids. The interaction between the drug and antigen-antibody binding sites on the surface of erythrocytes increases the sensitivity and specificity of these assays.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 240.05 g/mol
• Formel: C₉H₆BrNO₂
• Reinheit: Min. 95%
• InChl: InChI=1S/C9H6BrNO2/c10-5-11-8(12)6-3-1-2-4-7(6)9(11)13/h1-4H,5H2
• InChI Key: InChIKey=UUSLLECLCKTJQF-UHFFFAOYSA-N
• SMILES: O=C1c2ccccc2C(=O)N1CBr