2-(Methylsulfonyl)-5-(trifluoromethyl)-1,3,4-thiadiazole(CAS号:27603-25-4)
2-(甲基磺酰基)-5-(三氟甲基)-1,3,4-噻二唑
基本信息

CAS号
27603-25-4
分子式
C4H3F3N2O2S2
分子量
232.21 g/mol
Quick Actions
基本物理性质
沸点
269 ºC
闪点
116 ºC
折射率
1.465
安全信息
查看安全信息危险说明
H302-H315-H319-H335
同义词与参考文献
英文
- AKOS016005586
- FT-0759877
- 27603-25-4
- 1,3,4-Thiadiazole, 2-(methylsulfonyl)-5-(trifluoromethyl)-
- SY128065
- AMY7246
- MFCD04092021
- 2-methylsulphonyl-5-trifluoromethyl-1,3,4-thiadiazole
- 2-(Methylsulfonyl)-5-(trifluoromethyl)-1,3,4-thiadiazole
- EC 809-978-0
- N12315
- 2-methylsulfonyl-5-(trifluoromethyl)-1,3,4-thiadiazole
- DTXSID70865385
- NS00003209
- 1,3,4-Thiadiazole,2-(methylsulfonyl)-5-(trifluoromethyl)-
- 2-methanesulfonyl-5-(trifluoromethyl)-1,3,4-thiadiazole
- SCHEMBL2207938
- A26561
- EN300-221794
- 2-?(Methylsulfonyl)?-?5-?(trifluoromethyl)?-?1,?3,?4-?thiadiazole
- DS-16796
- 2-(Methylsulfonyl)-5-(Trifluormethyl)-1,3,4-Thiadiazol
- 2-(methylsulfonyl)-5-(trifluoromethyl)-1,3,4-t
- 2-(Methylsulfonyl)-5-(Trifluoromethyl)-1,3,4-Thiadiazol
- 2-methanesulfonyl-5-trifluoromethyl-[1,3,4]-thiadiazole
- ANW-65590
- CTK8C0971
- SureCN2207938
- C4H3F3N2O2S2
- 2-(trifluoromethyl)-5-(methylsulfonyl)-1,3,4-thiadiazole
- SQLPTSMJAQPVKR-UHFFFAOYSA-N
- X5558
- 2-methanesulfonyl-5
中文
- 2-甲砜基-5-三氟甲基-1,3,4-噻二唑
- 2-(甲基磺酰基)-5-(三氟甲基)-1,3,4-噻二唑
- 2-(甲磺酰基)-5-(三氟甲基)-1,3,4-噻二唑
MDL_Number
MFCD04092021
CAS号
27603-25-4
供应商信息
供应商名称 | 会员等级 | 认证状态 | 主要类别 | 最小订购量 | 操作 |
---|---|---|---|---|---|
相关文献
Synthesis of aviation fuel from bio-derived isophorone
Courtney Ford Ryan, Cameron M. Moore, Juan H. Leal, Troy A. Semelsberger, Jenny K. Banh, Junqing Zhu, Charles S. McEnally, Lisa D. Pfefferle, Andrew D. Sutton
DOI: 10.1039/C9SE01014A
Selective production of monocyclic aromatic hydrocarbons from ex situ catalytic fast pyrolysis of pine over the HZSM-5 catalyst with calcium formate as a hydrogen source
Kai Li, Ze-xiang Wang, Guan Zhang, Min-shu Cui, Qiang Lu, Yong-ping Yang
DOI: 10.1039/C9SE00605B
Building microsphere–nanosheet structures in N-doped carbon to improve its performance in the oxygen reduction reaction and vanadium redox flow batteries
Baobing Huang, Yuchuan Liu, Miao Xia, Jiugen Qiu, Zailai Xie
DOI: 10.1039/C9SE00851A
An overview of latest advances in exploring bioactive peptide hydrogels for neural tissue engineering
Pooja Sharma, Vijay Kumar Pal, Sangita Roy
DOI: 10.1039/D0BM02049D
Stabilizing synthetic DNA for long-term data storage with earth alkaline salts
A. Xavier Kohll, Philipp L. Antkowiak, Weida D. Chen, Bichlien H. Nguyen, Wendelin J. Stark, Luis Ceze, Karin Strauss, Robert N. Grass
DOI: 10.1039/D0CC00222D
Surface structure-dependent electrocatalytic reduction of CO2 to C1 products on SnO2 catalysts
Minling Fang, Zhiping Zheng, Jiayu Chen, Qian Chen, Deyu Liu, Binbin Xu, Jianyang Wu, Qin Kuang
DOI: 10.1039/C9SE00678H
Water-soluble pH-switchable cobalt complexes for aqueous symmetric redox flow batteries
Yuqiao Zhou
DOI: 10.1039/D0CC00383B
Increasing efficiency of perovskite solar cells using low concentrating photovoltaic systems
Hasan Baig, Hiroyuki Kanda, Abdullah M. Asiri, Mohammad Khaja Nazeeruddin, Tapas Mallick
DOI: 10.1039/C9SE00550A
Biomimetic hydrogels designed for cartilage tissue engineering
Alexander Stokes, Piergiorgio Gentile, Ana M. Ferreira
DOI: 10.1039/D0BM01852J
Development of wound healing scaffolds with precisely-triggered sequential release of therapeutic nanoparticles
Tauseef Ahmad, Sean McGrath, Catherine Sirafim, Ronaldo J. F. C. do Amaral, Shin-Loong Soong, Renuka Sitram, Shifa'a Turkistani, Francesco Santarella
DOI: 10.1039/D0BM01277G