(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]
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
The scavenger receptor CD36 facilitates the cellular uptake of long-chain fatty acids. As CD36-deficiency attenuates the development of high fat diet (HFD)-induced obesity, the role of CD36-deficiency in preadipocyte recruitment and adipocyte function was set out to characterize. Fat cell
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 thrombosis and haemostasis : JTH, 13(1), 126-135 (2014-10-28)
The autonomic nervous system attenuates inflammation through activation of the α7 nicotinic acetylcholine receptor (α7nAChR), a pathway termed the cholinergic anti-inflammatory reflex. Interestingly, α7nAChR is expressed on immune cells and platelets, both of which play a crucial role in the
On the Mechanism of the Thermal Rearrangement of 4-AlkyI-4H-1, 2, 4?Triazoles. Synthesis and Reaction of Optically Active
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