Melting point	-34.4 ºC
Boiling point	102-103 ºC (15 mmHg)
Flash point	110 ºC
Density	1.687
Refractive index	1.537-1.547

Symbol(GHS)	Xn
Hazard Codes	R22;R36/38
SDS/MSDS	S26;S37/39

Source	SDS/MSDS Samples
Alfa-Aesar	View & Download
Sigma-Aldrich	View & Download
TCI	View & Download

Synthetic Route

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Articles

Peer-Reviewed Papers

Synthesis of base-modified noraristeromycin derivatives and their inhibitory activity against human and Plasmodium falciparum recombinant S-adenosyl-L-homocysteine hydrolaseKitade Y, et al. Tetrahedron, 58(7), 1271-1277 (2002) Myers, A.G. et al. Tetrahedron Letters, 37, 3083-3083 (1996) Variable and stereoselective synthesis of azasugar analogues by a ruthenium-catalyzed ring rearrangementVoigtmann U and Blechert S Organic Letters, 2(25), 3971-3974 (2000) Theil, F. et al. Journal of the Chemical Society. Perkin Transactions 1, 255-255 (1996) An improved preparation of highly enantiomerically enriched (R)-(+)-4-tert-butyldimethylsiloxy-2-cyclopenten-1-oneMyers AG, et al. Tetrahedron Letters, 37(18), 3083-3086 (1996) (4R)-(+)-tert-Butyldimethylsiloxy-2-Cyclopenten-1-one: 2-Cyclopenten-1-one, 4-[[(1, 1-dimethylethyl) dimethylsilyl] oxy]-,(R)-Paquette LA, Organic Syntheses, 73(18), 36-36 (1996) Facile synthesis of 9-[(1′ R, 2′ S)-2′-hydroxy-3′-oxocyclopentan-1′-yl]-9-H-adenine possessing inhibitory activity against human recombinant S-adenosyl-l-homocysteine hydrolaseKitade Y, et al. Tetrahedron Letters, 42(3), 433-435 (2001) Design, synthesis, and anti-HIV activity of 4′-modified carbocyclic nucleoside phosphonate reverse transcriptase inhibitorsBoojamra CG, et al. Bioorganic & Medicinal Chemistry, 17(4), 1739-1746 (2009) Chemoenzymatic synthesis of carbocyclic nucleoside analogues with bicyclo [3.1. 0] hexyl residuesTheil F, et al. Journal of the Chemical Society. Perkin Transactions 1, 255-258 (1996) Paquette, L.A. et al. Organic Syntheses, 73, 36-36 (1995)

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