220639
3-噻吩乙酸
98%
别名:
噻吩-3-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:
230-166-1
Beilstein/REAXYS Number:
113622
MDL number:
Assay:
98%
Quality Level
assay
98%
mp
73-76 °C (lit.)
functional group
carboxylic acid
SMILES string
OC(=O)Cc1ccsc1
InChI
1S/C6H6O2S/c7-6(8)3-5-1-2-9-4-5/h1-2,4H,3H2,(H,7,8)
InChI key
RCNOGGGBSSVMAS-UHFFFAOYSA-N
General description
3-Thiopheneacetic acid acts as monocarboxylate ligand and forms oxo-carboxylate bridged digadolinium(III) complexes. Electrochemical oxidation of 3-thiopheneacetic acid in dry acetonitrile leads to the formation of a conducting polymeric film of poly (3-thiopheneacetic acid).
Application
3-Thiopheneacetic acid was used in:
- one-step, size control synthesis of gold nanoparticles
- in the preparation of gold nanoparticles capped with 3-thiopheneacetic acid (3-TAA) via borohydride reduction
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
Synthesis, density functional theory, molecular dynamics and electrochemical studies of 3-thiopheneacetic acid-capped gold nanoparticles.
Sosibo NM, et al.
Journal of Molecular Structure, 1006(1), 494-501 (2011)
Electrochemistry of poly (3-thiopheneacetic acid) in aqueous solution: evidence for an intramolecular chemical reaction.
Bartlett PN and Dawson DH.
Journal of Materials Chemistry, 4(12), 1805-1810 (1994)
One-step, shape control synthesis of gold nanoparticles stabilized by 3-thiopheneacetic acid.
Huang H and Yang X.
Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 255(1), 11-17 (2005)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 220639-10G | 04061838776525 |
| 220639-50G | 04061838776532 |