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2,5-Thiophenedicarboxaldehyde

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2,5-Thiophenedicarboxaldehyde Basic information

Product Name:
2,5-Thiophenedicarboxaldehyde
Synonyms:
  • TIMTEC-BB SBB000080
  • THIOPHENE-2,5-DICARBALDEHYDE
  • THIOPHENE-2,5-DICARBOXALDEHYDE
  • 2,5-THIOPHENEDICARBOXALDEHYDE
  • 2,5-Diformylthiophene
  • Thiophene-2,5-dialdehyde
  • 2,5-Thiophenedicarboxaldehyde,99%
  • 2,5-Thiophenedicarboxaldehyde 99%
CAS:
932-95-6
MF:
C6H4O2S
MW:
140.16
Product Categories:
  • Heterocyclic Compounds
  • Thiophenes & Benzothiophenes
  • Aldehydes
  • Building Blocks
  • Heterocyclic Building Blocks
  • Thiophenes
  • Thiophenes & Benzothiophenes
  • Thiophene
Mol File:
932-95-6.mol
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2,5-Thiophenedicarboxaldehyde Chemical Properties

Melting point:
115-117 °C (lit.)
Boiling point:
226.66°C (rough estimate)
Density 
1.327 (estimate)
refractive index 
1.5300 (estimate)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
solid
NIST Chemistry Reference
2,5-Thiophenedicarboxaldehyde(932-95-6)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29349990

MSDS

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2,5-Thiophenedicarboxaldehyde Usage And Synthesis

Chemical Properties

PALE BROWN-ORANGE TO PALE BROWN POWDER

Uses

2,5-Thiophenedicarboxaldehyde acts as a reagent in the synthesis of N,N''-bis-(mercaptophenylimine)thiophenedicarboxaldehyde Schiff base, and also functions as an intermediate in many organic synthesis.

Uses

2,5-Thiophenedicarboxaldehyde may be employed in the following studies:

  • Asymmetric synthesis of bis-homoallylic alcohols.
  • Synthesis of new symmetrical arylene bisimide derivatives.
  • As dialdehyde monomer in the synthesis of silicon-containing poly(p-phenylenevinylene)-related copolymers having uniform p-conjugated segment regulated by organosilicon units.
  • Synthesis of 2,5-bis[2-(5-N-isopropylamidino)benzimidazoyl]thiophene hydrochloride.

Synthesis Reference(s)

Synthesis, p. 316, 1988 DOI: 10.1055/s-1988-27553

General Description

2,5-Thiophenedicarboxaldehyde can be prepared from 2,5-bis(chloromethyl)thiophene by the application of Kr?hnke′s method.

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