Grundinformationen
- Standard-SMILES
O=C1OC(=O)c2cc(Br)cc3cccc1c23- InChIKey
LYXFXCSFCWZGNZ-UHFFFAOYSA-N- Summenformel
- C12H5BrO3
- Durchschnittliche Molmasse
- 277,07 g/mol
- Monoisotopische Masse
- 275,94220612
Namen und Bezeichner
- Bevorzugter Name
- 5-Bromobenzo[de]isochromene-1,3-dione
- IUPAC
- 7-bromo-3-oxatricyclo[7.3.1.05,13]trideca-1(12),5(13),6,8,10-pentaene-2,4-dione
- Englischer Name
- 3-Bromo-1,8-naphthalic anhydride
- Summenformel
- C12H5BrO3
- Molmasse
- 277.07
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
24050-49-5- PubChem CID
- 3907491
- DTXSID
DTXSID20397888- EC Number
- 681-858-9
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 3,2
- Polarare Oberfläche (TPSA)
- 43,4 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 3
- Frei drehbare Bindungen
- 0
- Schwere Atome
- 16
- Formalladung
- 0
- Komplexität
- 341
Physikochemische Eigenschaften
- Schmelzpunkt
- 244 · 244-246°C
- Siedepunkt
- 468.9 · 468.9±28.0 °C(Predicted)
- Dichte
- 1.812 · 1.812±0.06 g/cm3 (20 ºC 760 Torr)
- storage temp.
- Store at room temperature
- BRN
- 180001 · 180001
- InChI
- InChI=1S/C12H5BrO3/c13-7-4-6-2-1-3-8-10(6)9(5-7)12(15)16-11(8)14/h1-5H
- InChIKey
- LYXFXCSFCWZGNZ-UHFFFAOYSA-N
- SMILES
- C1(=O)OC(=O)C2=CC(Br)=CC3=C2C1=CC=C3
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Warning
H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 4 reports by companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Sicherheitsdaten
- risk_code
- 36/37/38
- safety_code
- 26-36
Chemie und Industrie
Anwendungen
Beschreibung3-Bromo-1,8-naphthalic anhydride is a naphthalic anhydride compound. Its structure incorporates a bromo functional group, meaning this product can participate in various chemical reactions and serve as a synthetic reagent for preparing photocatalysts, pharmaceutical preparations, or other organic heterocyclic compounds.
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