三(甲基硫代)甲烷
三(甲基硫代)甲烷结构式
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常用名 | 三(甲基硫代)甲烷 | 英文名 | tris(methylthio)methane |
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| CAS号 | 5418-86-0 | 分子量 | 154.31700 | |
| 密度 | 1.16 g/mL at 25ºC(lit.) | 沸点 | 102ºC15 mm Hg(lit.) | |
| 分子式 | C4H10S3 | 熔点 | 16ºC(lit.) | |
| MSDS | 中文版 美版 | 闪点 | 204 °F | |
| 符号 |
GHS07 |
信号词 | Warning |
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Catalytic enantioselective synthesis of naturally occurring butenolides via hetero-allylic alkylation and ring closing metathesis.
Org. Lett. 13(5) , 948-51, (2011) An efficient catalytic asymmetric synthesis of chiral γ-butenolides was developed based on the hetero-allylic asymmetric alkylation (h-AAA) in combination with ring closing metathesis (RCM). The synthetic potential of the h-AAA-RCM protocol was illustrated wi... |
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Research on L-nucleosides. Synthesis and biological evaluation of a series of L- and D-2',3'-dideoxy-3'-[tris(methylthio)methyl]-beta-pentofuranosyl nucleosides.
Bioorg. Med. Chem. 11(3) , 357-66, (2003) Novel nucleoside analogues of both D and L enantiomeric series were prepared by coupling reaction between a 2',3'-dideoxy-3'-modified furanose moiety and four different nucleobases. Though in all cases anomeric mixtures of nucleosides were obtained, the prese... |
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From ketones, aldehydes or alkyl halides to terminal 1, 1-difluoroolefins using BrF3. Hagooly A and Rozen S.
J. Fluor. Chem. 126(8) , 1239-45, (2005)
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