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Detail of > 93-44-7

  • CAS Number:
  • 93-44-7
  • Name:
  • 2-Naphthyl benzoate

  • Formula:
  • C17H12O2
  • Molecular Structure:
  • Synonyms:
  • 2-Naphthalenol,benzoate (9CI);2-Naphthol, benzoate (6CI,7CI,8CI);2-Benzoyloxynaphthalene;Benzonaphthol;Betabenzon;NSC 5537;Naphthalen-2-ylbenzoate;b-Naphthyl benzoate;2-Naphthalenol,2-benzoate;
  • Molecular Weight:
  • 248.28
  • EINECS:
  • 202-247-1
  • Density:
  • 1.199 g/cm3
  • Melting Point:
  • 105-109 °C
  • Boiling Point:
  • 413.5 °C at 760 mmHg
  • Flash Point:
  • 174.6 °C
  • Solubility:
  • insoluble in water
  • Appearance:
  • light brown crystalline powder
  • Safety:
  • 24/25Details
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CAS No. 

93-44-7 2-Naphthyl benzoate

Specificactions:Nafamostat mesylateCAS:82956-11-4
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93-44-7 2-Naphthyl benzoate

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CAS No. 

93-44-7 2-Naphthyl benzoate

Item name: Benzonaphtol CAS: 93-44-7 Molecular formula:C17H12O2 Molecular weight:248.276 Assay: 99.5% Appearance: white crystalline powder Package: 25kg/drum Shipment: General chemical
China (Mainland)   3502
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  • Address:Room 34-1 Xiaoshan Hangzhou China

CAS No. 

93-44-7 2-Naphthyl benzoate

2-Naphthyl Benzoate
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  • Tel:021-34979012 13311639313
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93-44-7 2-Naphthyl benzoate

β-Naphthyl Benzoate
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93-44-7 2-Naphthyl benzoate

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93-44-7 2-Naphthyl benzoate

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  • Tel:086-512-53640999
  • Address:Binghai Road, Chemical Development Zone, Taicang, Jiangsu Provice

CAS No. 

93-44-7 2-Naphthyl benzoate

2-NAPHTHYL BENZOATE
United States  
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  • Address:145 Witherspoon Street Princeton. NJ 08542

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93-44-7 2-Naphthyl benzoate

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93-44-7 2-Naphthyl benzoate

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    Reference

    Reactivity effect of active additives on the formation process of poly(ethylene terephthalate)
    Reactivity effect of active additives on the formation process of poly(ethylene terephthalate). Shevchenko, V. V. (Vses. Nauchno-Issled. Inst. Sint. Volokon, Kalinin, USSR). Prepr. - Mezhdunar. Simp. Khim. Voloknam, 2nd, Volume 1, 201-13. Program. Kom. Mezhdunar. Simp. Khim. Voloknam: Kalinin, USSR. (Russian) 1977. CODEN: 37KQAK. DOCUMENT TYPE: Conference CA Section: 35 (Synthetic High Polymers) The accelerating effect of bifunctional additives (terephthalic acid [100-21-0], di-Ph terephthalate [1539-04-4], and dinaphthyl terephthalate [58201-08-4]) on the rate of formation of poly(ethylene terephthalate) (I) [25038-59-9] was caused by the interaction of the additives (more reactive than the b-hydroxyethyl carboxylate groups) with b-hydroxyethyl carboxylate end groups of I. The latter interaction was studied on model compds. (ethylene glycol [107-21-1], benzoic acid [65-85-0], ethylene glycol monobenzoate [94-33-7], Ph benzoate [93-99-2], and b-naphthyl benzoate [93-44-7]). E.g., it was concluded that the rate consts. in the reactions of b-hydroxyethyl carboxylate end groups of I with aryl carboxylate groups of the accelerators were 11-13 times higher and the rate consts. in esterification of b-hydroxyethyl carboxylate end groups of I by the carboxylic groups of the accelerators were 4 times higher than the rate consts. of transesterification of the b-hydroxyethyl carboxylates.
    Plant growth stimulator
    Plant growth stimulator. Yukin, N. A.; Tsupikov, M. T. (Novocherkassk Institute of Melioration Engineering, USSR). U.S.S.R. SU 564844 15 Jul 1977 From: Otkrytiya, Izobret., Prom. Obraztsy, Tovarnye Znaki 1977, 54(26), 4. (Russian). (Union of Soviet Socialist Republics). CODEN: URXXAF. CLASS: IC: A01N005-00. APPLICATION: SU 76-2333860 3 Mar 1976. DOCUMENT TYPE: Patent CA Section: 5 (Agrochemicals) .beta.-Naphthyl benzoate (I) [93-44-7] is a plant growth stimulator.

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