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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

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

Storage Class Code

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

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)

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Soo Yei Ho et al.
Journal of medicinal chemistry, 60(15), 6678-6692 (2017-07-04)
Porcupine is an O-acyltransferase that regulates Wnt secretion. Inhibiting porcupine may block the Wnt pathway which is often dysregulated in various cancers. Consequently porcupine inhibitors are thought to be promising oncology therapeutics. A high throughput screen against porcupine revealed several

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