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108448-77-7 (1R)-(+)-2,10-Camphorsultam

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CAS： 108448-77-7 MDL Number： MFCD00151762 MF： C10H17NO2S MW： 215.31 Purity： >98% Product Description： Relevant Medicine Name： - COA SDS

Brand	CatalogID	Unit	Price($)	Your Price($)	Sale Price($)	Stock (US)	Stock (CN)	Ships within	Quantity	Buy
Accela	SY004517	1g	10.00	-	-	0	>5	3-5 days
Accela	SY004517	5g	15.00	-	-	0	5	3-5 days
Accela	SY004517	10g	20.00	-	-	0	4	3-5 days
Accela	SY004517	25g	27.00	-	-	0	>5	3-5 days
Accela	SY004517	100g	107.00	-	-	0	0	inquire
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Product InformationSafety InformationReferences

Flash point	150.3℃
Boiling point
Density
Storage	Light sensitive

Versatile chiral auxiliary introduced by Oppolzer. Review: Tetrahedron, 49, 293 (1993).
N-Acryloyl derivatives undergo enantioselective cycloaddition reactions: Helv. Chim. Acta, 67, 1397 (1984); Tetrahedron, 43, 1969 (1987). Hydrogenation of N-acryloyl derivatives proceeds with high diastereoselectivity: Tetrahedron Lett., 27, 183 (1986); Helv. Chim. Acta, 69, 1542 (1986), 69, 1817 (1986); 70, 1666 (1987). Induces asymmetric conjugate addition of Grignard reagents to N-acryloyl derivatives: Helv. Chim. Acta, 70, 2201 (1987). In the presence of strong bases, N-acyl derivatives undergo stereoselective alkylation: Tetrahedron Lett., 30, 5603 (1989); or aldol-type condensation reactions with aldehydes: J. Am. Chem. Soc., 112, 2767 (1990); Tetrahedron Lett., 32, 61 (1991).
Chiral auxiliary for the asymmetric Baylis-Hillman reaction: J. Am. Chem. Soc., 119, 4317 (1997).