332399
3-噻吩甲醇
98%
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关于此项目
经验公式（希尔记法）:
C5H6OS
化学文摘社编号:
分子量:
114.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
275-741-8
MDL number:
产品名称
3-噻吩甲醇, 98%
InChI key
BOWIFWCBNWWZOG-UHFFFAOYSA-N
InChI
1S/C5H6OS/c6-3-5-1-2-7-4-5/h1-2,4,6H,3H2
SMILES string
OCc1ccsc1
assay
98%
form
liquid
refractive index
n20/D 1.564 (lit.)
bp
86-88 °C/10 mmHg (lit.)
density
1.211 g/mL at 25 °C (lit.)
functional group
hydroxyl
Quality Level
Application
3-Thiophenemethanol was used in the preparation of 3-substituted thiophene conducting copolymers which has potential applications in electrochromic displays. It was also used in the synthesis of 4-(thiophene-3-ylmethoxy)phthalonitrile.
General description
Comparision of electrochemical polymerization properties of 3-thiophenemethanol and 3-methylthiophene has been reported.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
213.8 °F - closed cup
flash_point_c
101 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Electrochemical polymerization and characterization of new copolymers of 3-substituted thiophenes.
Alves MRA, et al.
Synthetic Metals, 160(1), 22-27 (2010)
Synthesis, molecular conformation, vibrational, electronic transition, and chemical shift assignments of 4-(thiophene-3-ylmethoxy) phthalonitrile: a combined experimental and theoretical analysis.
Coruh A, et al.
Structural Chemistry, 22(1), 45-56 (2011)
A comparative study of the electrochemistry of 3-thiophenemethanol and 3-methylthiophene.
Pohjakallio M and Sundholm G.
Synthetic Metals, 55(2), 1590-1595 (1993)
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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