S-Methyl 2-furancarbothioate | CAS No. 13679-61-3
Basic Information
CAS Number
13679-61-3
Molecular Formula
C6H6O2S
Molecular Weight
142.18 g/mol
Quick Actions
Basic Physical Properties
Boiling Point
63 ºC (at 2 mm Hg)
Flash Point
94 ºC
Refractive Index
1.5711
Classification & Uses
Chemical Classification
Safety Information
View Safety InformationSynonyms & References
English
- S-Methyl 2-Furancarbothioate
- 2-Furancarbothioic acid S-methylester
- Methyl 2-thiofuroate
- Methyl thiofuroate
- 2-Thiofuroic Acid S-Methyl Ester
- S-Methyl 2-Thiofuroate
- S-methyl furan-2-carbothioate
- CL057
- FEMA 3311
- METHYLTHIOL FUROATE
- S-METHYL THIOFUROATE
- methyl thio-2-furoate
- Mehtyl 2-thiolfuroate
- 2-Furancarbothioic Acid S-Methyl Ester
- Methyl 2-thiofuroate,97%
- 2-Furancarbothioic acid, S-methyl ester
- 2-Furoic acid, thio-, S-methyl ester
- S-Methyl thio-2-furoate
- 9H9BCF87R7
- FEMA No. 3311
- S-Methyl2-Furancarbothioate
- SCHEM
- METHYL THIOFUROATE
- METHYL 2-THIOFUROATE
- S-METHYL 2-THIOFUROATE
MDL_Number
MFCD00040266
CAS Number
13679-61-3
Customs_Code
2932190090
Supplier Information
| Supplier Name | Member Level | Authentication Status | Main Category | MOQ | Action |
|---|---|---|---|---|---|
 China - Jiangsu Xinxitai New Materials Co., Ltd. |
|||||
| China - Hubei De Ao Hua Yan Yiyao Technology Co., Ltd. |
|||||
| China - Hubei Meiban New Materials Co., Ltd. |
|||||
| China - Shanghai Yuyeh Biotechnology Co., Ltd. |
|||||
| China - Shijiazhuang Lide Chemicals Co., Ltd. |
|||||
| China - Jinan Xinliye Chemical Industry Co., Ltd. |
|||||
| China - Wuhan Eight Stars Biotechnology Co., Ltd. |
|||||
 Germany - Consic Software Engineering |
Related Compounds
![59156-70-6 - 1,1'-[(1,6-Dioxo-1,6-hexanediyl)bis(oxy)]di(2,5-pyrrolidinedione)](/structs/591/59156-70-6-0f4b.webp "59156-70-6 - 1,1'-[(1,6-Dioxo-1,6-hexanediyl)bis(oxy)]di(2,5-pyrrolidinedione)")
Recommended Journals
Related Articles
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
Efficient one-pot synthesis of alkyl levulinate from xylose with an integrated dehydration/transfer-hydrogenation/alcoholysis process
Mengmeng Wang, Xueying Gao, Liang He, Junhua Zhang
DOI: 10.1039/C9SE00982E
A model-based comparison of Ru and Ni catalysts for the Sabatier reaction
DOI: 10.1039/C9SE00787C
Illuminating endosomal escape of polymorphic lipid nanoparticles that boost mRNA delivery
Marco Herrera, Jeonghwan Kim, Yulia Eygeris, Antony Jozic
DOI: 10.1039/D0BM01947J
Visible light-driven cross-coupling reactions of alkyl halides with phenylacetylene derivatives for C(sp3)–C(sp) bond formation catalyzed by a B12 complex
Li Chen, Yohei Kametani, Kenji Imamura, Tsukasa Abe, Yoshihito Shiota, Kazunari Yoshizawa, Yoshio Hisaeda, Hisashi Shimakoshi
DOI: 10.1039/C9CC06185A
Transition-metal-free insertion reactions of alkynes into the C–N σ-bonds of imides: synthesis of substituted enamides or chromones
Zhong Zheng, Ye Wang, Murong Xu, Lingkai Kong, Mengdan Wang, Yanzhong Li
DOI: 10.1039/C8CC03059F
Life cycle assessment of power-to-gas with biogas as the carbon source
Xiaojin Zhang, Julia Witte, Tilman Schildhauer, Christian Bauer
DOI: 10.1039/C9SE00986H
Novel aqueous amine looping approach for the direct capture, conversion and storage of CO2 to produce magnesium carbonate
Meishen Liu, Hassnain Asgar, Soenke Seifert, Greeshma Gadikota
DOI: 10.1039/C9SE00316A
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