N-(Bromomethyl)phthalimide
CAS: 5332-26-3
Ref. 3D-FB75353
5g | To inquire | ||
10g | To inquire | ||
25g | To inquire | ||
50g | To inquire | ||
100g | To inquire |
Product Information
- 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
- See more synonyms
- N-(Bromomethyl)phthalimide,98+%
- N-Phthalimidomethyl Bromide
- NSC 3997
- Phthalimide, N-(bromomethyl)-
- Phthalimidomethyl Bromide
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.
Chemical properties
Technical inquiry about: 3D-FB75353 N-(Bromomethyl)phthalimide
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