1,3-Bis(methylthio)propane (CAS 24949-35-7)
QUICK LINKS
1,3-Bis(methylthio)propane is an intriguing organic compound classified as a cyclic compound. This colorless liquid exhibits a pleasant yet pungent odor. 1,3-Bis(methylthio)propane serves as a valuable reagent in synthesizing various compounds, including barbiturates, thiobarbiturates, and thiosemicarbazones. Moreover, it finds application in the synthesis of deuterated compounds and the preparation of organosulfur compounds. Additionally, Bis(methylthio)propane has been instrumental in the synthesis of novel organosulfur compounds, including thiols, thioesters, and thioketones. The mechanism of action of 1,3-Bis(methylthio)propane is reliant on the specific reaction it partakes in. Generally, when 1,3-Bis(methylthio)propane reacts with an appropriate acid or base, a new compound is formed. This reaction entails the cleavage of the carbon-sulfur bond and the subsequent formation of a fresh bond between the carbon and sulfur atoms.
1,3-Bis(methylthio)propane (CAS 24949-35-7) References
- Ferrocenyl derivatives with one, two, or three sulfur-containing arms for self-assembled monolayer formation. | Hu, J. and Mattern, DL. 2000. J Org Chem. 65: 2277-81. PMID: 10789435
- Thioether complexes of palladium(II) and platinum(II) as artificial peptidases. residue-selective peptide cleavage by a palladium(II) complex. | Stoffregen, SA., et al. 2005. Inorg Chem. 44: 8899-907. PMID: 16296845
- Gold(I)-dithioether supramolecular polymers: synthesis, characterization, and luminescence. | Awaleh, MO., et al. 2008. Inorg Chem. 47: 2964-74. PMID: 18366159
- Structure-property relationships of polyselenoethers [-(CH2)ySe-]x (y=1, 2, and 3) and related polyethers and polysulfides. | Sasanuma, Y., et al. 2008. J Phys Chem B. 112: 9613-24. PMID: 18646809
- Synthesis, Crystal Structures and Thermal Analysis of Two New Silver(I)–Dithioether Lamellar Coordination Polymers | , et al., (2009). Journal of Chemical Crystallography. volume 39: pages 122–127.
- Formation of cyclic ions in the electron impact induced fragmentation of 1,n-bis-(alkylthio) alkanes | , et al. (1990). Research on Chemical Intermediates. volume 13,: pages 17–29.
- Formation and characterization of 1-substituted 1,2-dithiolanyl radicals by laser flash photolysis | , et al. (1989). Research on Chemical Intermediates. volume 11,: pages 227–234.
- Mass spectral studies of some dithioethers and diamine-dithioethers | CA McAuliffe, FP McCullough, RD Sedgwick… - Inorganica Chimica …, 1978 - Elsevier. 1978,. Inorganica Chimica Acta. Volume 27,: Pages 185-189.
- Conformational Characteristics of Poly(trimethylene sulfide) and Structure−Property Relationships of Representative Polysulfides and Polyethers | Yuji Sasanuma and Akinori Watanabe. 2006,. Macromolecules. 39, 4,: 1646–1656.
- Synthesis, crystal structures and thermal analysis of two new coordination polymers | MO Awaleh, IG Farah, ES Dirieh, T Maris… - Comptes Rendus …, 2011 - Elsevier. November 2011,. Comptes Rendus Chimie. Volume 14, Issue 11,: Pages 991-996.
- Reactivity of 2-aryl-1,3-dithiane anions towards neopentyl, neophyl and phenyl iodides. New evidence for an SRN1 mechanism | and Gabriela Oksdath-Mansilla, Alicia B. Peñéñory. December 2011. Journal of Physical Organic Chemistry. Volume24, Issue12: Pages 1136-1143.
- Kinetics and thermal degradation of the fructose-methionine Amadori intermediates. GC-MS/SPECMA data bank identification of volatile aroma compounds☆ | G Vernin, J Metzger, C Boniface, MH Murello… - Carbohydrate …, 1992 - Elsevier. 4 June 1992,. Carbohydrate Research. Volume 230, Issue 1,: Pages 15-29.
- Oxidation of Dithia Compounds: Comparative Experimental and Theoretical Studies on 1,3-Bis(methylthio)propane, Bis(methylthio)methane, and meso-4,6-Dimethyl-1,3-dithiane | and M. Sc. Victorino Vallejos González, Prof. Dr. Joachim Podlech. October 21, 2021. European Journal of Organic Chemistry. Volume2021, Issue39: Pages 5430-5442.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1,3-Bis(methylthio)propane, 1 g | sc-265039 | 1 g | $121.00 |