295356-13-7

Basic information

• Product Name: (4S,4aR,5S,5aR,6R,12aS)-9-Amino-4-dimethylamino-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-8-phenyl-1,4,4a,5,5a,6,11,12a-octahydro-naphthacene-2-carboxylic acid amide
• Synonyms: (4S,4aR,5S,5aR,6R,12aS)-9-Amino-4-dimethylamino-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-8-phenyl-1,4,4a,5,5a,6,11,12a-octahydro-naphthacene-2-carboxylic acid amide
• CAS NO: 295356-13-7
• Molecular Weight: 535.554
• Mol File: 295356-13-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (4S,4aR,5S,5aR,6R,12aS)-9-Amino-4-dimethylamino-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-8-phenyl-1,4,4a,5,5a,6,11,12a-octahydro-naphthacene-2-carboxylic acid amide(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,4aR,5S,5aR,6R,12aS)-9-Amino-4-dimethylamino-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-8-phenyl-1,4,4a,5,5a,6,11,12a-octahydro-naphthacene-2-carboxylic acid amide(295356-13-7)
• EPA Substance Registry System: (4S,4aR,5S,5aR,6R,12aS)-9-Amino-4-dimethylamino-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-8-phenyl-1,4,4a,5,5a,6,11,12a-octahydro-naphthacene-2-carboxylic acid amide(295356-13-7)

Safety Data

• Hazardous Substances Data: 295356-13-7(Hazardous Substances Data)

Upstream product

• 295356-11-5 9-azidodoxycycline 
• 120793-45-5 <4S-(4α,12aα)>-4-(dimethylamino)-9-nitro-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide 
• 161321-34-2 <4S-(4α,12aα)>-9-amino-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide 
• 564-25-0 doxycycline 
• 960-16-7 tributylphenylstannane 
• 295356-12-6 9-amino-8-bromodoxycycline 

Relevant articles and documents

The synthesis of 8-substituted tetracycline derivatives, the first 8- position carbon-carbon bond

The synthesis of C8-functionalized tetracyclines using Stille coupling is described. These derivatives are the first reported with a carbon-carbon bond in the 8-position of a tetracycline negating total synthesis routes to 8-substituted tetracyclines. (C) 2000 Elsevier Science Ltd.