Grundinformationen
- Standard-SMILES
Cc1ccsc1- InChIKey
QENGPZGAWFQWCZ-UHFFFAOYSA-N- Summenformel
- C5H6S
- Durchschnittliche Molmasse
- 98,17 g/mol
- Monoisotopische Masse
- 98,01902119
Überblick
3-Methylthiophene is a member of thiophenes.
Namen und Bezeichner
- Bevorzugter Name
- 3-Methylthiophene
- IUPAC
- 3-methylthiophene
- Lokaler Name
- 3-Methylthiophen
- Englischer Name
- 3-Methylthiophene
- Summenformel
- C5H6S
- Molmasse
- 98.17
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
616-44-4- PubChem CID
- 12024
- DTXSID
DTXSID8060666- ChEBI
CHEBI:89007- UNII
- FK9ID0X5QV
- EC Number
- 210-482-6
- Nikkaji
- J37.034G
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 2,3
- Polarare Oberfläche (TPSA)
- 28,2 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 1
- Frei drehbare Bindungen
- 0
- Schwere Atome
- 6
- Formalladung
- 0
- Komplexität
- 43,2
Experimentelle und physikochemische Eigenschaften
LogP
2.34
2.34
Physical Description
Clear light yellow liquid; [Sigma-Aldrich MSDS]
Liquid
Physikochemische Eigenschaften
- Schmelzpunkt
- -69 °C · -69 °C (lit.)
- Siedepunkt
- 114 °C/738 · 114 °C/738 mmHg (lit.)
- Dichte
- 1.016 g/mL · 1.016 g/mL at 25 °C (lit.)
- Dampfdruck
- 42.4 mm · 42.4 mm Hg ( 37.7 °C)
- Brechungsindex
- 20 · n20/D 1.519(lit.)
- Flammpunkt
- 52 °F · 52 °F
- storage temp.
- Flammables area
- Löslichkeit
- 0.4 g/l · 0.40g/l
- Aggregatzustand
- Liquid
- Farbe
- Clear colorless to light yellow
- Wichte
- 1.016 · 1.016
- Wasserlöslichkeit
- insoluble
- BRN
- 1300 · 1300
- Henry's Law Constant
- 1.4 · 1.4×10-3 mol/(m3Pa) at 25℃, Duchowicz et al. (2020)
- Stabilität
- Volatile
- InChI
- 1S/C5H6S/c1-5-2-3-6-4-5/h2-4H,1H3
- InChIKey
- QENGPZGAWFQWCZ-UHFFFAOYSA-N
- SMILES
- Cc1ccsc1
- LogP
- 2.34 · 2.340
- CAS Datenbank
- 616 · 616-44-4(CAS DataBase Reference)
- NIST chemische Informationen
- 3 · Thiophene, 3-methyl-(616-44-4)
- EPA chemische Informationen
- 3 · Thiophene, 3-methyl- (616-44-4)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H225 (99.5%): Highly Flammable liquid and vapor [Danger Flammable liquids]
P210, P233, P240, P241, P242, P243, P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 188 reports by companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Regulatory Information
Chemical: Thiophene, 3-methyl-
Commission Regulation (EC) No 1565/2000 (Repealed by Com. Implementing Reg. (EU) No 872/2012)
Thiophene, 3-methyl-: Does not have an individual approval but may be used under an appropriate group standard
Toxikologische Informationen
Sicherheitsdaten
- F
- 8-10-13-23
- wgk
- 3
- tsca
- TSCA listed
- ridadr
- UN 1993 3/PG 2
- hs_code
- 29349990
- RTECS-Nr.
- XM9800000
- risk_code
- 11-20/22-36/37/38-37
- hazard_code
- F,Xn,Xi
- hazard_note
- Flammable/Harmful
- safety_code
- 7-16-29-33-36-37/39-26-7/9
- hazard_class
- 3
- packing_group
- II
- Speicherklasse
- 3 - Flammable liquids
- Hazard Classifications
- Flam. Liq. 2
Chemie und Industrie
Pharmakologische Informationen
Verwendung und Herstellung
Anwendungen
VerwendenThiophene, 2-methyIthiopheney and 3-methylthiophene act as inhibitors for the polymerization of trichloroethylene in a solvent used for the degreasing of iron and aluminum, said polymerization being catalyzed by contact of the solvent with the metals. Bonz, in 1885, reported the formation of a dichloroethylthiophene from chlorination of 2-ethylthiophene in the cold. Is Opolski studied the chlorination of 2- and 3-methylthiophenes, 2-ethyl- and 2-butylthiophene and reported constants for the monochloro derivatives. Voerman has chlorinated 3-methylthiophene in the side chain with phosphorus trichloride in the sunlight, but concurrent ring chlorination predominates. 3-Methylthiophene gives a unique reaction with alkyl- or arylsodium in which the substitution takes place exclusively in the 5-position rather than in the expected 2-position.
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