228796
3-噻吩乙醇
99%
别名:
2-(3-噻吩基)乙醇, 3-(2-羟乙基)噻吩
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关于此项目
经验公式（希尔记法）:
C6H8OS
化学文摘社编号:
分子量:
128.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
237-434-7
Beilstein/REAXYS Number:
107080
MDL number:
产品名称
3-噻吩乙醇, 99%
InChI key
YYPNNBPPDFTQFX-UHFFFAOYSA-N
InChI
1S/C6H8OS/c7-3-1-6-2-4-8-5-6/h2,4-5,7H,1,3H2
SMILES string
OCCc1ccsc1
assay
99%
form
liquid
refractive index
n20/D 1.552 (lit.)
bp
110-111 °C/14 mmHg (lit.)
density
1.144 g/mL at 25 °C (lit.)
functional group
hydroxyl
Quality Level
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Application
3-噻吩乙醇 [3-（2-羟乙基）噻吩] 用于合成多种醚和酯衍生物，如 3-（2-（苄氧基）乙基）噻吩、3-[2-（（三苯甲基）氧基）乙基] 噻吩、3-[2-（（三甲基硅烷基）氧基）乙基] 噻吩、3-[2-（二甲基叔丁基硅烷基）氧基）乙基] 噻吩、3-（2-乙酰氧基乙基）噻吩和 3-（2-（苯甲酰氧基）乙基）噻吩 。
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
197.6 °F - closed cup
flash_point_c
92 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Reactive groups on polymer-covered electrodes. 5. Synthesis and cyclovoltammetric analysis of 3-substituted thiophene derivatives.
Macromolecules, 30(24), 7419-7426 (1997)
Consuelo Ripoll et al.
Pharmaceutics, 13(2) (2021-03-07)
Recently, it was proposed that the thiophene ring is capable of promoting mitochondrial accumulation when linked to fluorescent markers. As a noncharged group, thiophene presents several advantages from a synthetic point of view, making it easier to incorporate such a
Yuwei Hao et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 19(16), 2046-2051 (2018-03-25)
Highly efficient cell capture and release with low background are urgently required for early diagnosis of diseases such as cancer. Herein, we report an electrochemical responsive superhydrophilic surface exhibiting specific cell capture and release with high yields and extremely low
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