所有图片(2)
别名:
2-(3-噻吩基)乙醇, 3-(2-羟乙基)噻吩
经验公式（希尔记法）:
C6H8OS
CAS号:
分子量:
128.19
Beilstein:
107080
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
质量水平
检测方案
99%
形式
liquid
折射率
n20/D 1.552 (lit.)
bp
110-111 °C/14 mmHg (lit.)
密度
1.144 g/mL at 25 °C (lit.)
SMILES字符串
OCCc1ccsc1
InChI
1S/C6H8OS/c7-3-1-6-2-4-8-5-6/h2,4-5,7H,1,3H2
InChI key
YYPNNBPPDFTQFX-UHFFFAOYSA-N
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应用
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 。
WGK
WGK 3
闪点(°F)
closed cup
闪点(°C)
closed cup
个人防护装备
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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