Molecular structure of α-Methyl-γ-butyrolactone, CAS Number: 1679-47-6
α-Methyl-γ-butyrolactone (CAS 1679-47-6)
Alternate Names:
4,5-Dihydro-3-methyl-2(3H)-furanone
CAS Number:
1679-47-6
Molecular Weight:
100.12
Molecular Formula:
C5H8O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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α-Methyl-γ-butyrolactone finds extensive application in the synthesis of diverse compounds, encompassing proteins and various chemicals. As a solvent, it facilitates a wide array of reactions, ranging from the synthesis of proteins to other chemical compounds. Additionally, it serves as a reagent in the synthesis of polymers.
α-Methyl-γ-butyrolactone (CAS 1679-47-6) References
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- An efficient synthesis of (+/-)-grandisol featuring 1,5-enyne metathesis. | Graham, TJ., et al. 2010. J Org Chem. 75: 226-8. PMID: 19957923
- Unusual C=C bond isomerization of an α,β-unsaturated γ-butyrolactone catalysed by flavoproteins from the old yellow enzyme family. | Durchschein, K., et al. 2012. Chembiochem. 13: 2346-51. PMID: 23024004
- Total synthesis and absolute configuration of curvularides A-E. | Sudhakar, G., et al. 2012. J Org Chem. 77: 10010-20. PMID: 23121599
- Combined experimental and theoretical study of the reactivity of γ-Butyro- and related lactones, with the OH radical at room temperature. | Barnes, I., et al. 2014. J Phys Chem A. 118: 5013-9. PMID: 24945977
- Functional annotation and structural characterization of a novel lactonase hydrolyzing D-xylono-1,4-lactone-5-phosphate and L-arabino-1,4-lactone-5-phosphate. | Korczynska, M., et al. 2014. Biochemistry. 53: 4727-38. PMID: 24955762
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- A Comprehensive Characterisation of Volatile and Fatty Acid Profiles of Legume Seeds. | Khrisanapant, P., et al. 2019. Foods. 8: PMID: 31817745
- Screening of Bacterial Quorum Sensing Inhibitors in a Vibrio fischeri LuxR-Based Synthetic Fluorescent E. coli Biosensor. | Qin, X., et al. 2020. Pharmaceuticals (Basel). 13: PMID: 32971993
- Sesquiterpene Lactones: Promising Natural Compounds to Fight Inflammation. | Matos, MS., et al. 2021. Pharmaceutics. 13: PMID: 34208907
- Effect of Inoculation with Lentilactobacillus buchneri and Lacticaseibacillus paracasei on the Maize Silage Volatilome: The Advantages of Advanced 2D-Chromatographic Fingerprinting Approaches. | Squara, S., et al. 2022. J Agric Food Chem. 70: 12232-12248. PMID: 36103255
- Grifolamine A, a novel bis-γ-butyrolactone from Grifola frondosa exerted inhibitory effect on α-glucosidase and their binding interaction: Affinity and molecular dynamics simulation. | Chen, S., et al. 2022. Curr Res Food Sci. 5: 2045-2052. PMID: 36345431
- Voltage-dependent calcium channels as targets for convulsant and anticonvulsant alkyl-substituted thiobutyrolactones. | Gross, RA., et al. 1997. J Pharmacol Exp Ther. 280: 686-94. PMID: 9023280
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
α-Methyl-γ-butyrolactone, 5 g | sc-253859 | 5 g | $87.00 | |||
α-Methyl-γ-butyrolactone, 25 g | sc-253859A | 25 g | $291.00 |