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MilliporeSigma

650080

Sigma-Aldrich

4-(Thiophen-3-yl)aniline

97%

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About This Item

Fórmula empírica (notación de Hill):
C10H9NS
Número de CAS:
Peso molecular:
175.25
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

form

solid

mp

99-103 °C (lit.)

SMILES string

Nc1ccc(cc1)-c2ccsc2

InChI

1S/C10H9NS/c11-10-3-1-8(2-4-10)9-5-6-12-7-9/h1-7H,11H2

InChI key

GYPDHLDQINBFPY-UHFFFAOYSA-N

Application

4-(Thiophen-3-yl)aniline can be used as a reactant to synthesize:
  • Pd(I)–poly[4-(thiophen-3yl)-aniline] composite material by in situ polymerization and composite formation method.
  • Schiff base, 2-methoxy-6-[(4-thiophene-3-yl-phenylimino)-methyl]-phenol by condensation reaction with o-vanillin.
  • 2-(1H-Imidazol-1-yl)-N-(4-(thiophen-3-yl)phenyl)acetamide by reacting with 2-(1H-imidazol-1-yl)acetic acid using HATU as amide coupling agent.

pictograms

Skull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Single step synthesis of a polymer supported palladium composite: a potential anode catalyst for the application of methanol oxidation
Siwal S, et al.
Royal Society of Chemistry Advances, 6(53), 47212-47219 (2016)
Synthesis, characterization, and magnetic and thermal studies on some metal (II) thiophenyl schiff base complexes
Osowole AA
International Journal of Inorganic Chemistry, 2011 (2011)

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