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Sigma-Aldrich

2-Thiopheneethylamine

96%

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About This Item

Fórmula empírica (Notação de Hill):
C6H9NS
Número CAS:
Peso molecular:
127.21
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

Ensaio

96%

Formulário

liquid

índice de refração

n20/D 1.551 (lit.)

p.e.

200-201 °C/750 mmHg (lit.)

densidade

1.087 g/mL at 25 °C (lit.)

grupo funcional

amine

cadeia de caracteres SMILES

NCCc1cccs1

InChI

1S/C6H9NS/c7-4-3-6-2-1-5-8-6/h1-2,5H,3-4,7H2

chave InChI

HVLUYXIJZLDNIS-UHFFFAOYSA-N

Descrição geral

2-Thiopheneethylamine (2-(thiophen-2-yl)ethanamine) is an aromatic amine. It undergoes microwave induced condensation with iminodiacetic acid to form the corresponding piperazine-2,6-dione derivatives. Its effect as a probable substitute to the pyridine ligand on the performance of poly(3-hexylthiophene)/CdSe hybrid solar cells has been investigated.

Aplicação

2-Thiopheneethylamine (2-thiophene ethyl amine, 2-(thien-2-yl)ethylamine) is suitable to functionalize multiwall carbon nanotubes (MWCNT).
It may be used as a reactant in the synthesis of pyrimidine derivatives by reacting with various isothiocyanatoketones and acylguanidines derivatives by reacting with aroyl S-methylisothiourea.

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Classificações de perigo

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

190.4 °F - closed cup

Ponto de fulgor (°C)

88 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Veera Sadhu et al.
Nanotechnology, 22(26), 265607-265607 (2011-05-18)
We have successfully prepared mono- and bi-functionalized multiwall carbon nanotubes (MWCNT) with thiophene, amine and thiophene-amine groups. The dispersion of nanotubes has been enhanced and stable optimized dispersions in organic solvents were obtained. These functionalized nanotubes have been successfully incorporated
Efficient synthesis of piperazine-2,6-dione and 4-(1H-indole-2-carbonyl) piperazine-2,6-dione derivatives and their evaluation for anticancer activity.
Kumar S, et al.
Medicinal Chemistry Research, 22(10), 4600-4609 (2013)
Synthesis, anti-inflammatory and analgesic activity evaluation of some pyrimidine derivatives.
Sondhi SM, et al.
Indian J. Chem. B, 48(2), 273-273 (2009)
S Padmanabhan et al.
Bioorganic & medicinal chemistry letters, 11(24), 3151-3155 (2001-11-27)
Solution-phase synthesis of various acylguanidine derivatives and the evaluation of a small library of compounds as potential sodium channel blockers are described.
Jun Yan Lek et al.
ACS applied materials & interfaces, 3(2), 287-292 (2011-01-26)
For hybrid solar cells, interfacial chemistry is one of the most critical factors for good device performance. We have demonstrated that the size of the surface ligands and the dispersion of nanoparticles in the solvent and in the polymer are

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