| Other Names | 135-65-9, 3-Hydroxy-3'-nitro-2-naphthanilide, 3-Hydroxy-N-(3-nitrophenyl)-2-naphthamide, Naphthol AS-BS, Azoic Coupling Component 17, Acna Naphthol M, 3-hydroxy-N-(3-nitrophenyl)naphthalene-2-carboxamide, Amarthol AS-BS, Irganaphthol RM, Naphtanilide BS, Dragonthol BS, Naphtazol B, Naphthanil BS, Naphthoide BS, Naphtoelan BS, Azoground BS, Azonaphtol MNA, Solunaptol MNL, Acco Naphthol AS-BS, Brenthol MN, Kambothol ASBS, Diathol BS, Naphthol AS-BS Supra, Celcot RM, Naftolo MBS, Azotol MNA, Azotol NMA, Tulathol AS-BS, Ultrazol IV-BS, Daito Grounder BS, Naphtol AS-BS, 3-Hydroxy-N-(3-nitrophenyl)-2-naphthalenecarboxamide, Anthonaphthol AS-BS, Hiltonaphthol AS-BS, Mitsui Naphthozol BS, Naptanilide BS Supra, Naphtol AS-BS Supra, Cibanaphthol RM, Amanil Naphthol AS-BS, Naphthol AS-BS Dispersible, 2-Naphthalenecarboxamide, 3-hydroxy-N-(3-nitrophenyl)-, C.I. Azoic Coupling Component 17, 2-naphthanilide, UNII-8K775B2J7E, 2-Naphthanilide, 3-hydroxy-3'-nitro-, DTXSID3044544, C.I. 37515, EINECS 205-209-2, NSC 37168, NSC-37168, CHEMBL65374, 2-Hydroxy-3-naphthoic Acid m-Nitroanilide, MLS000738144, DTXCID1024544, 8K775B2J7E, NSC37168, 2-HYDROXY-3'-NITRO-3-NAPHTHANILIDE, 2-HYDROXY-3-NAPHTHOIC ACID 3-NITROANILIDE, MFCD00021637, Oprea1_145295, cid_67277, SCHEMBL2743106, YZJSKRBKHCLMQC-UHFFFAOYSA-N, HMS2750J18, Tox21_301464, BDBM50091995, PNU-26370, 3-hydroxy-2-naphthoic m-nitroanilide, 3-Hydroxy-3\'-nitro-2-naphthanilide, AKOS015914160, AKOS040744527, NCGC00246934-01, NCGC00255765-01, CAS-135-65-9, SMR000393904, 3-HYDROXY-3'-NITRO-2-NAPTHANILIDE, CS-0206908, H0314, MLS000738144-02, NS00021001, 2-Naphthanilide, 3-hydroxy-3'-nitro-(8CI), D90835, MLS-0292193.0001, SR-01000200944, SR-01000200944-1, (3-Hydroxy(2-naphthyl))-N-(3-nitrophenyl)carboxamide, Q27270667, 3-Hydroxy-naphthalene-2-carboxylic acid (3-nitro-phenyl)-amide, 205-209-2 |
|---|---|
| IUPAC Name | 3-hydroxy-N-(3-nitrophenyl)naphthalene-2-carboxamide |
| CAS | 106910-83-2 |
| Molecular Weight | 308.29 |
| Molecular Formula | C17H12N2O4 |
| SMILES | C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC(=CC=C3)[N+](=O)[O-])O |




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