Grundinformationen
- Standard-SMILES
OB(O)c1cncc(Cl)c1- InChIKey
NJXYBTMCTZAUEE-UHFFFAOYSA-N- Summenformel
- C5H5BClNO2
- Durchschnittliche Molmasse
- 157,36 g/mol
- Monoisotopische Masse
- 157,01018648
Namen und Bezeichner
- Bevorzugter Name
- 5-Chloropyridine-3-boronic acid
- IUPAC
- (5-chloro-3-pyridinyl)boronic acid
- Englischer Name
- (5-Chloropyridin-3-yl)boronic acid
- Summenformel
- C5H5BClNO2
- Molmasse
- 157.36
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
872041-85-5- PubChem CID
- 20111877
- DTXSID
DTXSID70602590- EC Number
- 677-212-0
Eigenschaften
Berechnete Struktureigenschaften
- Polarare Oberfläche (TPSA)
- 53,4 Ų
- H-Brücken-Donoren
- 2
- H-Brücken-Akzeptoren
- 3
- Frei drehbare Bindungen
- 1
- Schwere Atome
- 10
- Formalladung
- 0
- Komplexität
- 114
Physikochemische Eigenschaften
- Schmelzpunkt
- 255 · 255-260℃
- Siedepunkt
- 335.3 · 335.3±52.0 °C(Predicted)
- Dichte
- 1.41 · 1.41±0.1 g/cm3(Predicted)
- storage temp.
- 2 · 2-8°C
- Aggregatzustand
- powder
- pka
- 5.91 · 5.91±0.10(Predicted)
- Farbe
- White
- InChI
- 1S/C5H5BClNO2/c7-5-1-4(6(9)10)2-8-3-5/h1-3,9-10H
- InChIKey
- NJXYBTMCTZAUEE-UHFFFAOYSA-N
- SMILES
- OB(O)c1cncc(Cl)c1
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Warning
H315 (98%): 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 49 reports by companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Sicherheitsdaten
- wgk
- 3
- hs_code
- 2933399990
- risk_code
- 36/37/38
- hazard_code
- Xi
- safety_code
- 26
- Speicherklasse
- 11 - Combustible Solids
- Hazard Classifications
- Eye Irrit. 2Skin Irrit. 2STOT SE 3
Chemie und Industrie
Anwendungen
Verwenden5-Chloro-3-pyridineboronic acid can be used as an intermediate:In the preparation of positron emission tomography (PET) radioligand [11C]MK-1064, which is applicable in the orexin-2 receptor imaging.In the synthesis of orexin 2 receptor antagonist (2-SORA) MK-1064.In the preparation of pyridyl-cycloalkyl derived microsomal prostaglandin E synthase-1 inhibitors.In the synthesis of ATAD2 bromodomain inhibitors.
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