195944
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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-639-8
Beilstein/REAXYS Number:
114551
MDL number:
产品名称
2-噻吩乙酸, 98%
InChI key
SMJRBWINMFUUDS-UHFFFAOYSA-N
InChI
1S/C6H6O2S/c7-6(8)4-5-2-1-3-9-5/h1-3H,4H2,(H,7,8)
SMILES string
OC(=O)Cc1cccs1
assay
98%
form
powder
bp
160 °C/22 mmHg (lit.)
mp
63-64 °C (lit.)
Quality Level
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Application
2-Thiopheneacetic acid was used in the preparation of rosette-like nanoscale Au materials.
General description
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.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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)
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)
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
Manuel Temprado et al.
The journal of physical chemistry. A, 112(41), 10378-10385 (2008-09-26)
The enthalpies of formation in the condensed and gas states, Delta f H m degrees (cd) and Delta f H m degrees (g), of 2- and 3-thiopheneacetic acids were derived from their respective enthalpies of combustion in oxygen, measured by
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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