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650080

Sigma-Aldrich

4-(Thiophen-3-yl)aniline

97%

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About This Item

Empirical Formula (Hill Notation):
C10H9NS
CAS Number:
Molecular Weight:
175.25
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Soo Yei Ho et al.
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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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