CAS 716-39-2
:Anidride 2,3-naftalendicarbossilica
- 1,3-ββ-Isonaphthofurandione
- 2,3-Naphthalenedicarboxylic acid anhydride
- 2,3-Naphthalenedicarboxylic anhydride
- 2,3-Naphthalic anhydride
- Naphtho[2,3-C]Furan-1,3-Dione
Naphtho[2,3-c]furan-1,3-dione
CAS:Formula:C12H6O3Purezza:95%Colore e forma:SolidPeso molecolare:198.1742Naphtho[2,3-c]furan-1,3-dione
CAS:Naphtho[2,3-c]furan-1,3-dionePurezza:99%Peso molecolare:198.18g/mol2,3-Naphthalenedicarboxylic Anhydride
CAS:Formula:C12H6O3Purezza:>95.0%(GC)(T)Colore e forma:White to Gray to Brown powder to crystalPeso molecolare:198.182,3-Naphthalic Anhydride
CAS:Prodotto controllatoStability Moisture Sensitive
Applications 2,3-Naphthalic anhydride is used as a reagent to synthesize analogues of Thalidomide (T338850), an inhibitor of tumour necrosis factor that was once abandoned because it caused birth defects, but is currently used as an inhibitor of angiogenesis in patients with multiple myeloma.
References D’Amato, R., et al.: Proc. Nat. Acad. Sci., 91, 4082 (1994); Ehrenpreis, E., et al.: Gastroenterology, 117, 1271 (1999); Parma, T., et al.: Nat. Med., 5, 582 (1999); Singhal, S., et al.: New Engl. J. Med., 341, 1565 (1999)Formula:C12H6O3Colore e forma:NeatPeso molecolare:198.172,3-Naphthalic Anhydride
CAS:2,3-Naphthalic anhydride is a naphthalene derivative that can be used to synthesize amides, amines and other organic compounds. It is obtained by the reaction of 2,3-dihydroxynaphthalene with a metal halide such as chloride or bromide. This reaction produces 2,3-naphthalic anhydride in high yield. The compound has been used as a precursor for the fluorescent derivative naphthofluorescein and propiolic acid. A synthetic process for this compound was first developed in 1887 by R. Pinner and L. Hahn. The compound has been found to have numerous applications in the production of plastics, textiles and dyes.
Formula:C12H6O3Purezza:Min. 95%Peso molecolare:198.17 g/mol





