3-Thiophenecarboxaldehyde

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 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
color Clear yellow to light brown
Specific Gravity1.228
Water Solubility Not miscible in water.
Sensitive Air Sensitive
BRN 105889
InChIKeyRBIGKSZIQCTIJF-UHFFFAOYSA-N
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 T
HazardClass AIR SENSITIVE
HS Code 29339900
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.
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
ETHYL 2-AMINO-5-ETHYLTHIOPHENE-3-CARBOXYLATE 3-Acetyl-2,5-dichlorothiophene ETHYL 2-AMINO-4-METHYLTHIOPHENE-3-CARBOXYLATE 5-CHLORO-BENZO[B]THIOPHENE-3-CARBOXYLIC ACID 2-AMINO-4,5,6,7-TETRAHYDRO-BENZO[B]THIOPHENE-3-CARBOXYLIC ACID METHYL ESTER 4-KETO-4,5,6,7-TETRAHYDROTHIANAPHTHENE 4-[(4-CHLOROPHENYL)THIO]THIOPHENE-3-CARBOXYLIC ACID 3-Acetyl-2,5-dimethylthiophene 3-Acetylthiophene METHYL 4-[(4-CHLOROPHENYL)THIO]THIOPHENE-3-CARBOXYLATE 3-Thiophenecarboxaldehyde 2,5-DICHLOROTHIOPHENE-3-CARBONYL CHLORIDE Thiophene-2,3-dicarboxylic acid 4,4,4-trifluoro-1-thiophen-3-yl-butane-1,3-dione DIETHYL 5-AMINO-3-METHYL-2,4-THIOPHENEDICARBOXYLATE ETHYL 2-[(2-CHLOROACETYL)AMINO]-4,5,6,7-TETRAHYDRO-1-BENZOTHIOPHENE-3-CARBOXYLATE METHYL 2,5-DICHLOROTHIOPHENE-3-CARBOXYLATE Cephalothin sodium

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