(R)-(−)-2-Butanol can be used as a reagent in the synthesis of:
1-[(S)-2-butyl]-3,5 diphenyl-1H-1,2,4 triazole from 3,5 diphenyl-1H-1,2,4 triazole by Mitsunobu reaction.[1]
2-butyl tosylate building block by reacting with toluenesulfonyl chloride.[2]
(R)-(-)-2-Butanol has been used as a freeze drying medium during the long term cryopreservation of smooth muscle cells samples in a freezing container.[3]
Murine cerebrovascular cells as a cell culture model for cerebral amyloid angiopathy: isolation of smooth muscle and endothelial cells from mouse brain
Thiazolidinediones reduce hepatic steatosis and increase HDL cholesterol levels. In mice with human-like lipoprotein metabolism (APOE*3-Leiden.CETP transgenic mice), a decrease in hepatic triglyceride content is associated with a decrease in plasma cholesteryl ester transfer protein (CETP) mass and an increase
Low birth weight may be associated with high levels of cholesterol in later life through genetic factors that affect both birth weight and cholesterol metabolism. Alterations in cholesterol synthesis and absorption may play an important role in this association. We
Stereochemistry of trifluoroacetolysis of optically active 2-Butyl Tosylate. A test for hydrogen bridging
Allen AD, et al.
The Journal of Organic Chemistry, 48(24), 4527-4530 (1983)
Journal of the American Society for Mass Spectrometry, 28(12), 2686-2691 (2017-09-25)
Here we report on the gas-phase interactions between protonated enantiopure amino acids (L- and D-enantiomers of Met, Phe, and Trp) and chiral target gases [(R)- and (S)-2-butanol, and (S)-1-phenylethanol] in 0.1-10.0 eV low-energy collisions. Two major processes are seen to
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