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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
  • 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
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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.)
Flash point:
165 °F
storage temp. 
2-8°C
solubility 
Chloroform, Hexanes
form 
Liquid
Specific Gravity
1.228
color 
Clear yellow to light brown
Water Solubility 
Not miscible in water.
Sensitive 
Air Sensitive
BRN 
105889
InChIKey
RBIGKSZIQCTIJF-UHFFFAOYSA-N
LogP
1.010
CAS DataBase Reference
498-62-4(CAS DataBase Reference)
NIST Chemistry Reference
3-Thiophenecarboxaldehyde(498-62-4)
EPA Substance Registry System
3-Thiophenecarboxaldehyde (498-62-4)
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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

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3-Thiophenecarboxaldehyde Usage And Synthesis

Chemical Properties

clear yellow to light brown liquid

Uses

3-Thiophenecarboxaldehyde is used in biological studies to determine the volatile compounds formed from the interaction between organoselenium and sulfur compounds.

Definition

ChEBI: 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

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