Grundinformationen
- Standard-SMILES
COc1ccc(C(C)C)cc1B(O)O- InChIKey
UTKAEAGLVJFBMK-UHFFFAOYSA-N- Summenformel
- C10H15BO3
- Durchschnittliche Molmasse
- 194,04 g/mol
- Monoisotopische Masse
- 194,11142474
Namen und Bezeichner
- Bevorzugter Name
- 5-Isopropyl-2-methoxyphenylboronic acid
- IUPAC
- (2-methoxy-5-propan-2-ylphenyl)boronic acid
- Englischer Name
- 5-Isopropyl-2-methoxybenzeneboronic acid
- Summenformel
- C10H15BO3
- Molmasse
- 194.04
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
216393-63-4- PubChem CID
- 4589190
- DTXSID
DTXSID40404609- EC Number
- 681-890-3
Eigenschaften
Berechnete Struktureigenschaften
- Polarare Oberfläche (TPSA)
- 49,7 Ų
- H-Brücken-Donoren
- 2
- H-Brücken-Akzeptoren
- 3
- Frei drehbare Bindungen
- 3
- Schwere Atome
- 14
- Formalladung
- 0
- Komplexität
- 173
Physikochemische Eigenschaften
- Schmelzpunkt
- 84 · 84-88 °C
- Siedepunkt
- 350 · 350.0±52.0 °C(Predicted)
- Dichte
- 1.08 · 1.08±0.1 g/cm3(Predicted)
- storage temp.
- 2 · 2-8°C
- pka
- 8.6 · 8.60±0.58(Predicted)
- BRN
- 9193266 · 9193266
- InChI
- 1S/C10H15BO3/c1-7(2)8-4-5-10(14-3)9(6-8)11(12)13/h4-7,12-13H,1-3H3
- InChIKey
- UTKAEAGLVJFBMK-UHFFFAOYSA-N
- SMILES
- COc1ccc(cc1B(O)O)C(C)C
- CAS Datenbank
- 216393 · 216393-63-4(CAS DataBase Reference)
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
- wgk
- 3
- hs_code
- 2931900090
- risk_code
- 36/37/38
- safety_code
- 26-36
- Speicherklasse
- 13 - Non Combustible Solids
Chemie und Industrie
Anwendungen
Verwenden5-Isopropyl-2-Methoxybenzeneboronic acid can be used as reactant involved in the synthesis of many biologically active molecules including Oxazolidinones for use as cholesteryl ester transfer protein inhibitors for atherosclerosis treatment; Selective quinazolinyl-phenol inhibitors of CHK1 as antitumor and radioprotectants; Biaryl-containing carbamates as CETP inhibitors and α -Sulfone hydroxamates as MMP inhibitors5Reactant involved in Suzuki-Miyaura cross coupling with 2-nitroarenediazonium tetrafluoroborate for synthesis of 2-nitrobiphenyls.
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