![]() 4-BUTYROTHIOLACTONE structure
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Common Name | 4-BUTYROTHIOLACTONE | ||
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CAS Number | 1003-10-7 | Molecular Weight | 102.15500 | |
Density | 1.206g/cm3 | Boiling Point | 197.4ºC at 760mmHg | |
Molecular Formula | C4H6OS | Melting Point | 138 °C | |
MSDS | Chinese USA | Flash Point | 87.6ºC | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
A Novel Synthesis of Poly(ester-alt-sulfide)s by the Ring-Opening Alternating Copolymerization of Oxiranes with gamma-Thiobutyrolactone Using Quaternary Onium Salts or Crown Ether Complexes as Catalysts.
Macromolecules 31(15) , 4746-52, (1998) Poly(ester-alt-sulfide) (polymer 1) was synthesized by the alternating copolymerization of glycidyl phenyl ether (GPE) with gamma-thiobutyrolactone (TBL) catalyzed by either quaternary onium salts or crown ether complexes. The copolymerization proceeded to pr... |
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Metabolic response against sulfur-containing heterocyclic compounds by the lignin-degrading basidiomycete Coriolus versicolor.
Appl. Microbiol. Biotechnol. 58(4) , 517-26, (2002) The fungal conversions of sulfur-containing heterocyclic compounds were investigated using the lignin-degrading basidiomycete Coriolus versicolor. The fungus metabolized a series of sulfur compounds--25 structurally related thiophene derivatives--via several ... |
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Mechanism of hydrolysis and aminolysis of homocysteine thiolactone.
Chemistry 12(15) , 4144-52, (2006) Homocysteine thiolactone (tHcy) is deemed a risk factor for cardiovascular diseases and strokes, presumably because it acylates the side chain of protein lysine residues ("N-homocysteinylation"), thereby causing protein damage and autoimmune responses. We ana... |
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Structure-activity studies of fluoroalkyl-substituted gamma-butyrolactone and gamma-thiobutyrolactone modulators of GABA(A) receptor function.
Bioorg. Med. Chem. 6(1) , 43-55, (1998) Dihydro-2(3H)-furanones (gamma-butyrolactones) and dihydro-2(3H)-thiophenones (gamma-thiobutyrolactones) containing fluoroalkyl groups at positions C-3, C-4, and C-5 of the heterocyclic rings were prepared. The anticonvulsant/convulsant activities of the comp... |
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Alkyl-substituted gamma-butyrolactones act at a distinct site allosterically linked to the TBPS/picrotoxinin site on the GABAA receptor complex.
Brain Res. 615(1) , 170-4, (1993) Effects of alkyl-substituted gamma-butyrolactones and gamma-thiobutyrolactones on [35S]t-butylbicyclophosphorothionate (35S-TBPS) dissociation from the picrotoxinin receptor were studied. Unlike picrotoxinin, these lactones accelerated the dissociation rate o... |
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Phytogrowth-inhibitory activities of sulfur-containing compounds. II. The inhibitory activities of thiosalicylic acid and dihydro-2(3H)-thiophenone-related compounds on plant growth.
Biol. Pharm. Bull. 16(8) , 813-6, (1993) Thiosalicylic acid (I) showed rather strong inhibitory activity on the growth of roots of all plants treated except Abelmoschus esculentus Moench at the concentration of 5.0 x 10(-4) M. This compound strongly inhibited the growth of the root of Echinochloa ut... |
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Tiny droplets make a big splash.
Nature Methods 3(2) , 71, (2006)
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One-pot difunctionalization of poly (ω-pentadecalactone) with thiol-thiol or thiol-acrylate groups, catalyzed by Candida antarctica lipase B. Takwa M, et al.
Macromol. Rapid Commun. 27(22) , 1932-1936, (2006)
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