3-thiophene carboxaldehyde

3-formylthiophene

CAS: 498-62-4 C5 H4 O S MW: 112.15108000

Identification

Name3-thiophene carboxaldehyde
CAS Number498-62-4
EINECS207-865-5
FDA UNIISearch
Molecular FormulaC5 H4 O S
Molecular Weight112.15108000
MDL NumberMFCD00005466
Nikkaji NumberJ149.677H
Beilstein1932694
XlogP31.00 (est)

Regulatory

Physical Properties

Appearance colorless to pale yellow clear liquid (est)
Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 1.23000 to 1.23500 @ 20.00 °C.
Pounds per Gallon - (est). 10.247 to 10.288
Refractive Index 1.58200 to 1.58600 @ 20.00 °C.
Boiling Point 194.00 to 196.00 °C. @ 760.00 mm Hg, 190.00 to 191.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure 0.537000 mmHg @ 25.00 °C. (est)
Flash Point 165.00 °F. TCC ( 73.90 °C. )
logP (o/w) 1.010
Soluble in water, 1.468e+004 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for 3-thiophene carboxaldehyde usage levels up tonot for fragrance use.
Recommendation for 3-thiophene carboxaldehyde flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

cognac PMC

Synonyms

3- formyl thiophene 3- formylthiophene 3- thenaldehyde 3- thienophenecarboxyaldehyde 3- thiophenaldehyde thiophene-3-carbaldehyde thiophene-3-carboxaldehyde 3- thiophenealdehyde 3- thiophenecarbaldehyde 3- thiophenecarboxaldehyde PubMed: Characterization of volatile components and odor-active compounds in the oil of edible mushroom Boletopsis leucomelas. PubMed: The development of a one pot, regiocontrolled, three-component reaction for the synthesis of thieno[2,3-c]pyrroles. PubMed: A biotinylated undecylthiophene copolymer bioconjugate for surface immobilization: creating an alkaline phosphatase chemiluminescence-based biosensor. PubMed: Synthesis and carbonic anhydrase inhibitory activity of 4-substituted 2-thiophenesulfonamides. PubMed: Synthesis and structure-activity relationships among glycosidic derivatives of 4'-demethylepipodophyllotoxin and epipodophyllotoxin, showing VM26- and VP16-213-like activities.