Hoffer's chlorosugar is a protected chlorinated sugar derivative used as an intermediate in the synthesis of nucleosides. Its structure features two 4-methylbenzoyl ester groups and a chlorine atom at the anomeric position.
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CAS 4330-21-6
1-Chloro-3,5-di(4-chlorbenzoyl)-2-deoxy-D-ribose
pharmaceutical intermediate
3,5-dichloro-4-nitropyridine
pharmaceutical intermediate
7-dehydrocholesterol
pharmaceutical intermediate
1H-benzimidazol-2-ylmethanethiol
pharmaceutical intermediate
5-Formyltetrahydropteroic acid
pharmaceutical intermediate
1-Chloro-3,5-di-O-toluoyl-2-deoxy-D-ribofuranose
pharmaceutical intermediate
2-Deoxy-alpha-D-erythropentofuranose 1-acetate 3,5-bis(4-chlorobenzoate)
pharmaceutical intermediate
2-Deoxy-2,2-difluoro-alpha-D-erythro-pentofuranose 3,5-dibenzoate 1-methanesulfonate
pharmaceutical intermediate
[(2R,3S,5R)-5-chloro-3-(4-methylbenzoyl)oxyoxolan-2-yl]methyl 4-methylbenzoate
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CC1=CC=C(C=C1)C(=O)OC[C@@H]2[C@H](C[C@H](O2)Cl)OC(=O)C3=CC=C(C=C3)C