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
EINECS:
Product Categories:Heterocyclic Compounds;Thiophenes & Benzothiophenes;Aldehydes;Building Blocks;Heterocyclic Building Blocks;Thiophenes;Thiophenes & Benzothiophenes;Thiophene
Mol File:932-95-6.mol
2,5-Thiophenedicarboxaldehyde Structure
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 Reference2,5-Thiophenedicarboxaldehyde(932-95-6)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HS Code 29349990
MSDS Information
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2,5-Thiophenedicarboxaldehyde English
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ACROS English
2,5-Thiophenedicarboxaldehyde Usage And Synthesis
Chemical PropertiesPALE BROWN-ORANGE TO PALE BROWN POWDER
Uses2,5-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.
Uses2,5-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 Description2,5-Thiophenedicarboxaldehyde can be prepared from 2,5-bis(chloromethyl)thiophene by the application of Kr?hnke′s method.
2,5-Thiophenedicarboxaldehyde Preparation Products And Raw materials
Preparation Products2,5-Bis(5-tert-butyl-2-benzoxazolyl)thiophene
Thianaphthene RARECHEM AL BO 0664 2-Thenaldehyde Protiofate 5-Acetylthiophene-2-carboxylic acid 3,4-Dihydroxy-thiophene-2,5-dicarboxylic acid dimethyl ester 2,5-Dicarboxylic acid-3,4-ethylenedioxythiophene 3-Thiophenecarboxaldehyde CHEMBRDG-BB 6969221 2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE-5,7-DICARBALDEHYDE THIOPHENE-2,5-DICARBOXYLIC ACID DISODIUM SALT 2,5-Thiophenedicarboxaldehyde Dibenzothiophene Thifensulfuron methyl 2,5-Thiophenedicarboxylic acid 5-FORMYL-2-THIOPHENECARBOXYLIC ACID Tetrahydrothiophene Cephalothin sodium

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