NSC50684
dc.creator | US National Cancer Institute | en_GB |
dc.date.accessioned | 2005-08-22T14:03:54Z | |
dc.date.available | 2005-08-22T14:03:54Z | |
dc.date.created | 2003-02-01 | en_GB |
dc.date.issued | 2005-08-22T14:03:54Z | |
dc.format.extent | 5883 bytes | |
dc.format.extent | 5612 bytes | |
dc.format.mimetype | chemical/x-cml | |
dc.format.mimetype | chemical/x-cml | |
dc.identifier | NSC50684 | en_GB |
dc.identifier.ichi | C17H12ClNO2,18-13-5H-7H-14(8H-6H-13)19H-17(20)15-9H-11-3H-1H-2H-4H-12(11)10H-16(15)21H | en_GB |
dc.identifier.inchi | InChI=1S/C17H12ClNO2/c18-13-5-7-14(8-6-13)19-17(21)15-9-11-3-1-2-4-12(11)10-16(15)20/h1-10,20H,(H,19,21) | |
dc.identifier.inchikey | OHAXNCGNVGGWSO-UHFFFAOYSA-N | |
dc.identifier.uri | http://www.dspace.cam.ac.uk/handle/1810/50108 | |
dc.language.iso | en_GB | |
dc.publisher | Unilever Center for Molecular Informatics, Cambridge University | en_GB |
dc.title | NSC50684 | en_GB |
dc.title.alternative | Acna Naphthol PC | en_GB |
dc.title.alternative | Amanil Naphthol AS-E | en_GB |
dc.title.alternative | Amarthol AS-E | en_GB |
dc.title.alternative | Azoic Coupling Component 10 | en_GB |
dc.title.alternative | C.I. Azoic Coupling Component 10 | en_GB |
dc.title.alternative | C.I. 37510 | en_GB |
dc.title.alternative | Cibanaphthol RC | en_GB |
dc.title.alternative | Daito Grounder E | en_GB |
dc.title.alternative | Hiltonaphthol AS-E | en_GB |
dc.title.alternative | Naphtanilide E | en_GB |
dc.title.alternative | Naphtazol E | en_GB |
dc.title.alternative | Naphthol ACNA PC | en_GB |
dc.title.alternative | Naphthol AS-E | en_GB |
dc.title.alternative | Naphtoelan E | en_GB |
dc.title.alternative | Naphtol AS-E Supra | en_GB |
dc.title.alternative | Sanatol E | en_GB |
dc.title.alternative | Tulathol AS-E | en_GB |
dc.title.alternative | 2-Naphthalenecarboxamide, N-(4-chlorophenyl)-3-hydroxy- (9CI) | en_GB |
dc.title.alternative | 2-Naphthanilide, 4'-chloro-3-hydroxy- (8CI) | en_GB |
dc.type | Chemical Structures | en_GB |