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5381-20-4

5381-20-4 Structure

5381-20-4 Structure
IdentificationMore
[Name]

1-Benzothiophene-3-carbaldehyde
[CAS]

5381-20-4
[Synonyms]

1-BENZOTHIOPHENE-3-CARBALDEHYDE
1-BENZOTHIOPHENE-3-CARBOXALDEHYDE
BENZO[B]THIOPHENE-3-CARBOXALDEHYDE
BUTTPARK 154\50-70
RARECHEM AM LA 0006
THIANAPHTHENE-3-CARBOXALDEHYDE
BENZOTHIOPHENE-3-CARBOXALDEHYDE
Benzo[B]Thiophene-3-Carboxalde
3-Benzo[b]thiophenecarbaldehyde
Benzo[b]thiophene-3-carbaldehyde
[EINECS(EC#)]

611-051-9
[Molecular Formula]

C9H6OS
[MDL Number]

MFCD00052376
[Molecular Weight]

162.21
[MOL File]

5381-20-4.mol
Chemical PropertiesBack Directory
[Appearance]

Yellow to brown crystalline powder
[Melting point ]

53-57 °C (lit.)
[Boiling point ]

166 °C/20 mmHg (lit.)
[density ]

1.2123 (rough estimate)
[refractive index ]

1.5500 (estimate)
[Fp ]

>230 °F
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[λmax]

302nm(EtOH)(lit.)
[CAS DataBase Reference]

5381-20-4(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HS Code ]

29349990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Diethyl ether-->N,N-Dimethylformamide-->Chloroform-->Government regulation-->n-Butyllithium-->Thianaphthene-->BENZO[B]THIOPHENE-2-CARBOXALDEHYDE-->Formaldehyde
[Preparation Products]

N-methyl-benzo[b]thiophene-3-methanamine
Hazard InformationBack Directory
[Chemical Properties]

Yellow to brown crystalline powder
[Uses]

Thianaphthene-3-carboxaldehyde (Benzo[b]thiophene-3-carboxaldehyde) may be used as a starting material in the multi-step synthesis of anthra[2,3-b:7,6-b′]bis[1benzothiophenes (ABBTs).
It may be used in the synthesis of :
  • 6-(N,N-dimethylamino)-2-(benzo[b]thiophen-3-yl)quinazolin-4-one
  • 6-(pyrrolidin-1-yl)-2-(benzo[b]thiophen-3-yl)quinazolin-4-one
  • (Z)-2-(benzo-[b]-thio-phen-3-yl-methyl-ene)-1-aza-bi-cyclo-[2.2.2]-octan-3-one
[General Description]

Thianaphthene-3-carboxaldehyde, also known as benzo[b]thiophene-3-carboxaldehyde, can be synthesized from 3-methyl-benzo[b]thiophene. It undergoes phosphine-free palladium coupling with aryl halides to form 2-arylbenzo[b]thiophenes.
Spectrum DetailBack Directory
[Spectrum Detail]

1-Benzothiophene-3-carbaldehyde(5381-20-4)IR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Thianaphthene-3-carboxaldehyde, 95%(5381-20-4)
[Sigma Aldrich]

5381-20-4(sigmaaldrich)
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