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Merck
CN

195944

Sigma-Aldrich

2-噻吩乙酸

98%

别名:

噻吩-2-乙酸

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关于此项目

经验公式(希尔记法):
C6H6O2S
化学文摘社编号:
分子量:
142.18
Beilstein:
114551
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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质量水平

方案

98%

表单

powder

沸点

160 °C/22 mmHg (lit.)

mp

63-64 °C (lit.)

SMILES字符串

OC(=O)Cc1cccs1

InChI

1S/C6H6O2S/c7-6(8)4-5-2-1-3-9-5/h1-3H,4H2,(H,7,8)

InChI key

SMJRBWINMFUUDS-UHFFFAOYSA-N

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一般描述

Adsorption of 2-thiopheneacetic acid on XAD-4, NDA-100 and ND-90 resin has been investigated. A new polymeric complex of Cu(II) and 2-thiopheneacetic acid has been synthesized and characterized by IR and Raman spectroscopy.

应用

2-Thiopheneacetic acid was used in the preparation of rosette-like nanoscale Au materials.

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Study of Adsorption of 2-Thiopheneacetic Acid on Three Adsorbent Resins.
Wei R, et al.
Acta Polymerica Sinica / Gao Fen Zi Xue Bao, 4, 471-477 (2004)
Synthesis, X-ray crystal structure and vibrational spectra of a polymeric copper (II) complex with 2-thiopheneacetic acid.
Drozdzewski P, et al.
Polyhedron, 23(10), 1785-1792 (2010)
Z Boulsourani et al.
Materials science & engineering. C, Materials for biological applications, 76, 1026-1040 (2017-05-10)
Seeking for copper based metallo-therapeutics, three triple bridged dinuclear copper(II) complexes [Cu
Cláudia Sg Gomes et al.
Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986), 93(7), 1901-1915 (2018-07-17)
The extraction of biopharmaceuticals from plasma and serum often employs overly complicated antiquated procedures that can inflict serious damage on especially prone protein targets and which afford low purification power and overall yields. This paper describes systematic development of a
Hye-Seon Shin et al.
ACS applied materials & interfaces, 5(4), 1429-1435 (2013-01-23)
Rosette-like nanoscale Au materials were simply prepared through one-pot reduction of the AuCl₄⁻ precursor by 2-thiopheneacetic acid (2-TAA) without extra surface capping ligands at room temperature. 2-TAA underwent polymerization into polythiophene derivatives while the AuCl₄⁻ precursor was simultaneously reduced into

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