Detail of > 132-68-3
- CAS Number:
- 132-68-3
- Name:
2-Naphthalenecarboxamide,3-hydroxy-N-1-naphthalenyl-
- Superlist Name:
- 3-Hydroxy-N-naphthalen-1-ylnaphthalene-2-carboxamide
- Formula:
- C21H15NO2
- Molecular Structure:

- Synonyms:
- 2-Naphthamide,3-hydroxy-N-1-naphthyl- (6CI,7CI,8CI);2-Hydroxy-3-naphthoic acid a-naphthylamide;2-Hydroxynaphthalene-3-carboxylicacid a-naphthylamide;3-Hydroxy-N-1-naphthyl-2-naphthamide;Acna Naphthol F;Amanil Naphthol AS-BO;Amarthol AS-BO;Anthonaphthol M 3B;Azoic Coupling Component 4;Azonaphtol AN;Azotol ANF;C.I. 37560;Cibanaphthol RN;Conazoic D;Dragonthol BO;Dycosthol AS-BO;Hebeithol AS-BO;Hiltonaphthol AS-BO;KiwaGrounder BO;N-(1-Naphthyl)-3-hydroxy-2-naphthamide;Naftol AS-BS;Naftolo MBO;Naphtanilide BO;Naphtazol 3B;Naphthoide BO;Naphthol AS-BO;Naphthol BO;Naphtoelan BO;Naphtol AS-BO;Napthol ASBO;Solunaptol ANL;Tulathol AS-BO;Ultrazol VII-BO;
- Molecular Weight:
- 313.35
- EINECS:
- 205-075-5
- Density:
- 1.333 g/cm3
- Melting Point:
- 222-223 °C
- Boiling Point:
- 479.3 °C at 760 mmHg
- Flash Point:
- 243.6 °C
- Deleted CAS:
- 58391-86-9
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Reference
- Bisazo compounds
- Bisazo compounds. (Konishiroku Photo Industry Co., Ltd., Japan). Jpn. Kokai Tokkyo Koho JP 58144358 A2 27 Aug 1983 Showa, 12 pp. (Japanese). (Japan). CODEN: JKXXAF. CLASS: IC: C07C121-78; C09B035-039; G03G005-06. APPLICATION: JP 82-27821 22 Feb 1982. DOCUMENT TYPE: Patent CA Section: 25 (Benzene, Its Derivatives, and Condensed Benzenoid Compounds) Section cross-reference(s): 74 Bisazo compds. I (R = N:NR1; R1 = Q, Q1, Q2; Z = atoms to form an arom. or heterocyclic ring; R2 = aryl, or heterocyclyl; R3 = H, alkyl, aryl; R4 = alkyl, aralkyl, aryl), useful as photoconductors, were prepd. by treating tetrazonium salts I (R = N:N+ X-; X- = anion) with QH, Q1H or Q2H. Thus, refluxing 2,7-dinitrofluroenone with CH2(CN)2 in C6H6, adding AcOH and piperidine and refluxing the mixt. 2 h gave 65% I (R = NO2), redn. of which by refluxing with Sn and HCl 1 h gave 95.8% I (R = NH2.HCl). Diazotization by HCl, NaNO2 and NH4PF6 gave I (R = N:N+ PF6-) (II). Treating 2-hydroxy-3-naphthanilide in DMF with N(CH2CH2OH)3 and II 1 h at 5° and 2 h at room temp. 132-68-3 and 88701-07-9 are just another two chemicals used in this study. gave 83% I R = Q3). .
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