3-Thiophenecarboxaldehyde CAS 498-62-4

Introduction:Basic information about 3-Thiophenecarboxaldehyde CAS 498-62-4, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

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;THIOPHENE-3-CARBALDEHYDE
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;Carbonyl Compounds;Aromatic Aldehydes & Derivatives (substituted);Aldehydes;Thiophenes & Benzothiophenes;Thiophene&Benzothiophene;Heterocyclic Compounds;Miscellaneous;Thiophens;Thiophenes;Heterocycles;Thiophenes & Benzothiophenes;bc0001
Mol File:498-62-4.mol

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
color Clear yellow to light brown
Specific Gravity1.228
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

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

3-Thiophenecarboxaldehyde Preparation Products And Raw materials

Preparation Products(5-BROMOTHIOPHEN-3-YL)METHANESULFONYL CHLORIDE-->2-(3-THIENYL)ETHANAMINE-->2-NITROTHIOPHENE-4-CARBOXALDEHYDE-->3,4-Dithia-7H-cyclopenta[a]pentalene-->4,4-Dihexyl-4H-cyclopenta[1,2-b:5,4-b']dithiophene-->3-Thiophenecarboxaldehyde, 5-chloro--->THIENO[2,3-B]THIOPHENE-->METHYL 3-THIOPHENECARBOXYLATE 97-->3-(3-thienyl)pentanedioic acid-->FURAN-2-YL(THIOPHEN-3-YL)METHANOL-->1-(3-Thienyl)butane-1,2-dione-->Thiophene, 3-(2,2-dibromoethenyl)--->PHENYLAMINO-THIOPHEN-3-YL-ACETONITRILE
3-Thiophenecarbonyl chloride CAS 41507-35-1
3-Trifluoromethylbenzylcyanide CAS 2338-76-3
Recommended......
TOP