2,5-Thiophenedicarboxaldehyde
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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MSDS
- Language:English Provider:2,5-Thiophenedicarboxaldehyde
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
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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.
2,5-ThiophenedicarboxaldehydeSupplier
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2,5-Thiophenedicarboxaldehyde(932-95-6)Related Product Information
- 3-Thiophenecarboxaldehyde
- Thianaphthene
- Thifensulfuron methyl
- Dibenzothiophene
- 2-Thiophenecarboxaldehyde
- Tetrahydrothiophene
- Cephalothin sodium
- 5-FORMYL-2-THIOPHENECARBOXYLIC ACID
- 2,5-Dicarboxylic acid-3,4-ethylenedioxythiophene
- 5-Acetylthiophene-2-carboxylic acid
- 3,4-Dihydroxy-thiophene-2,5-dicarboxylic acid dimethyl ester
- 2,5-Thiophenedicarboxylic acid
- 5-ACETYL-2-THIOPHENECARBALDEHYDE
- METHYL 5-FORMYL-2-THIOPHENECARBOXYLATE
- 2,3-THIOPHENEDICARBOXALDEHYDE,THIOPHENE-2,3-DICARBALDEHYDE
- THIOPHENE-2,5-DICARBOXYLIC ACID DISODIUM SALT
- 2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE-5,7-DICARBALDEHYDE
- 2,5-Thiophenedicarboxylic acid dimethyl ester