Grundinformationen
- Standard-SMILES
O=Cc1ccccn1- InChIKey
CSDSSGBPEUDDEE-UHFFFAOYSA-N- Summenformel
- C6H5NO
- Durchschnittliche Molmasse
- 107,11 g/mol
- Monoisotopische Masse
- 107,03711378
Überblick
2-formylpyridine is a pyridinecarbaldehyde that is pyridine in which the hydrogen at position 2 is replaced by a formyl group.
Namen und Bezeichner
- Bevorzugter Name
- 2-Pyridinecarboxaldehyde
- IUPAC
- pyridine-2-carbaldehyde
- Lokaler Name
- Pyridin-2-carbaldehyd
- Englischer Name
- 2-Pyridinecarboxaldehyde
- Summenformel
- C6H5NO
- Molmasse
- 107.11
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
1121-60-4、26445-06-7- PubChem CID
- 14273
- DTXSID
DTXSID1061522- ChEMBL
CHEMBL274794- ChEBI
CHEBI:73012- UNII
- KH86K8FHZ2
- EC Number
- 214-333-6
- Nikkaji
- J28.014C
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 0,4
- Polarare Oberfläche (TPSA)
- 30 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 2
- Frei drehbare Bindungen
- 1
- Schwere Atome
- 8
- Formalladung
- 0
- Komplexität
- 82,6
Experimentelle und physikochemische Eigenschaften
Physikochemische Eigenschaften
- Schmelzpunkt
- -21 · -21--22°C
- Siedepunkt
- 181 °C · 181 °C(lit.)
- Dichte
- 1.126 g/mL · 1.126 g/mL at 25 °C(lit.)
- Dampfdruck
- 73 Pa · 73Pa at 20℃
- Brechungsindex
- 20 · n20/D 1.536(lit.)
- Flammpunkt
- 130 °F · 130 °F
- storage temp.
- 2 · 2-8°C
- Aggregatzustand
- liquid (strong colored)
- pka
- 3.8 · 3.8(at 20℃)
- Farbe
- Clear yellow to yellow-brown
- PH
- 6.5 · 6.5 (111g/l, H2O, 20℃)
- Wasserlöslichkeit
- miscible
- BRN
- 105341 · 105341
- InChI
- 1S/C6H5NO/c8-5-6-3-1-2-4-7-6/h1-5H
- InChIKey
- CSDSSGBPEUDDEE-UHFFFAOYSA-N
- SMILES
- [H]C(=O)c1ccccn1
- LogP
- 0.714 at · 0.714 at 20.5℃
- CAS Datenbank
- 1121 · 1121-60-4(CAS DataBase Reference)
- NIST chemische Informationen
- 2 · 2-Pyridinecarboxaldehyde(1121-60-4)
- EPA chemische Informationen
- 2 · 2-Pyridinecarboxaldehyde (1121-60-4)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H226 (17.1%): Flammable liquid and vapor [Warning Flammable liquids]
P210, P233, P240, P241, P242, P243, P260, P261, P264, P264+P265, P270, P271, P272, P273, P280, P284, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P303+P361+P353, P304+P340, P305+P354+P338, P316, P317, P319, P320, P321, P330, P332+P317, P333+P317, P362+P364, P363, P370+P378, P391, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 76 reports by companies from 16 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Regulatory Information
Chemical: 2-Pyridinecarboxaldehyde
Status: Cease Manufacture Update: 10-05-2019 https://echa.europa.eu/registration-dossier/-/registered-dossier/25571
2-Pyridinecarbaldehyde: Does not have an individual approval but may be used under an appropriate group standard
Hazards Summary
An irritant that may cause serious eye injury; May cause skin sensitization; Harmful by ingestion; Toxic by inhalation; [Alfa Aesar MSDS] Search for (1121-60-4[EC/RN Number]) AND (sensitizer OR sensitization OR allergic) found no results; [PubMed) See Pyridine.
Toxikologische Informationen
Sicherheitsdaten
- F
- 8-10-23
- wgk
- 3
- tsca
- TSCA listed
- ridadr
- UN 1989 3/PG 3
- hs_code
- 29333999
- risk_code
- 10-22-36/37/38-51/53-46-43-34-23-52
- hazard_code
- Xn,Xi,N,T,F
- hazard_note
- Irritant/Keep Cold/Air Sensitive
- safety_code
- 7-26-36-61-53-45-36/37/39-29-16-36/37
- hazard_class
- 6.1
- packing_group
- III
- Speicherklasse
- 6.1A - Combustible acute toxic Cat. 1 and 2very toxic hazardous materials
- Hazard Classifications
- Acute Tox. 2 InhalationAcute Tox. 4 OralEye Dam. 1Skin Corr. 1BSkin Sens. 1
Chemie und Industrie
Verwendung und Herstellung
Anwendungen
Verwenden2-Pyridinecarboxaldehyde has been used:To synthesize chitosan based bifunctionalized adsorbent.In the aldol addition reaction with pyruvate in the presence of 2-keto-3-deoxy-6-phosphogluconate aldolase (KDPG) catalyst to form (S)-4-hydroxy-2-keto-4-(2′-pyridyl)butyrate.In the condensation reaction with (S)-()-α-methylbenzylamine and (R)-(+)-α-methylbenzylamine to synthesize two chiral (S)-()- and (R)-(+)Schiff base compounds.It can also be combined with thiosemicarbazide to form 2-pyridinecarboxaldehyde thiosemicarbazone ligand (L) which can further complex with Ni(II) and Cu(II) salts (MX) to form [M(L)2X2] complexes.
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Vorgelagerte Rohstoffe
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Ergänzende Hinweise
DefinitionChEBI: 2-Pyridinecarboxaldehyde is a pyridinecarbaldehyde that is pyridine in which the hydrogen at position 2 is replaced by a formyl group.
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