Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

650080

Sigma-Aldrich

4-(Thiophen-3-yl)aniline

97%

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Empirical Formula (Hill Notation):
C10H9NS
CAS Number:
834884-74-1
Molecular Weight:
175.25
MDL number:
MFCD06740168
UNSPSC Code:
12352100
PubChem Substance ID:
24883728
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

Related Categories

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
GHS06

Signal Word

Danger

Hazard Statements

H301,H315,H319,H335

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)

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service