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3-Thiophenecarboxaldehyde

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3-Thiophenecarboxaldehyde Basic information
Product Name:3-Thiophenecarboxaldehyde
Synonyms:3-THIOPHENE CARBOXALDEHYDE 98%;3-THIOPHENECARBOXALDEHYDE;3-THIOPHENALDEHYDE;3-THIOPHENEALDEHYDE;3-THIOPHENECARBALDEHYDE;RARECHEM AM LA 0011;THIOPHENE-3-ALDEHYDE;TIMTEC-BB SBB004320
CAS:498-62-4
MF:C5H4OS
MW:112.15
EINECS:207-865-5
Product Categories:Building Blocks;Heterocyclic Building Blocks;Functional Materials;Reagents for Conducting Polymer Research;Thiophene Derivatives (for Conduting Polymer Research);Thiophen;Aldehydes;Thiophenes & Benzothiophenes;Thiophene&Benzothiophene;Heterocyclic Compounds;Miscellaneous;Thiophens;Aromatic Aldehydes & Derivatives (substituted);Carbonyl Compounds;Heterocycles;bc0001;Thiophenes & Benzothiophenes;Thiophenes
Mol File:498-62-4.mol
3-Thiophenecarboxaldehyde Structure
3-Thiophenecarboxaldehyde Chemical Properties
Melting point -30 °C
Boiling point 194-196 °C (lit.) 86-87 °C/20 mmHg (lit.)
density 1.28 g/mL at 25 °C (lit.)
vapor pressure 0.31 mm Hg ( 20 °C)
refractive index n20/D 1.583(lit.)
Fp 165 °F
storage temp. 2-8°C
solubility Chloroform, Hexanes
form Liquid
Specific Gravity1.228
color Clear yellow to light brown
Water Solubility Not miscible in water.
Sensitive Air Sensitive
BRN 105889
InChI1S/C5H4OS/c6-3-5-1-2-7-4-5/h1-4H
InChIKeyRBIGKSZIQCTIJF-UHFFFAOYSA-N
SMILES[H]C(=O)c1ccsc1
LogP1.010
CAS DataBase Reference498-62-4(CAS DataBase Reference)
NIST Chemistry Reference3-Thiophenecarboxaldehyde(498-62-4)
EPA Substance Registry System3-Thiophenecarboxaldehyde (498-62-4)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-43-36/37/38
Safety Statements 37-24-36-26-36/37/39-20/21
WGK Germany 3
Autoignition Temperature>392 °F
Hazard Note Irritant
TSCA TSCA listed
HazardClass AIR SENSITIVE
HS Code 29339900
Storage Class10 - Combustible liquids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
ProviderLanguage
3-Thiophenecarboxaldehyde English
ACROS English
SigmaAldrich English
ALFA English
3-Thiophenecarboxaldehyde Usage And Synthesis
Chemical Propertiesclear yellow to light brown liquid
Uses3-Thiophenecarboxaldehyde is used in biological studies to determine the volatile compounds formed from the interaction between organoselenium and sulfur compounds.
Application3-Thiophenecarboxaldehyde is a versatile organic compound known for its unique thiophene ring structure, which imparts distinct chemical properties. This compound is widely utilized in the synthesis of various pharmaceuticals and agrochemicals, making it a valuable building block in organic chemistry.
DefinitionChEBI: An aldehyde that is thiophene substituted by a formyl group at position 3.
Synthesis Reference(s)Journal of Medicinal Chemistry, 16, p. 1361, 1973 DOI: 10.1021/jm00270a009
Organic Syntheses, Coll. Vol. 4, p. 918, 1963
Tag:3-Thiophenecarboxaldehyde(498-62-4) Related Product Information
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