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Detail of "24758-49-4"

  • CAS Number:
  • 24758-49-4
  • Name:
  • Methanone,[4-(4-morpholinyl)phenyl]phenyl-

  • Molecular Structure:
  • Formula:
  • C17H17NO2
  • Molecular Weight:
  • 267.32
  • Synonyms:
  • Benzophenone,4-morpholino- (8CI);4-Morpholinobenzophenone;(4-Morpholin-4-yl-phenyl)-phenyl-methanone;NSC 111168;[4-(Morpholin-4-yl)phenyl](phenyl)methanone;
  • EINECS:
  • 246-447-7
  • Density:
  • 1.157 g/cm3
  • Melting Point:
  • 142-145 °C
  • Boiling Point:
  • 450.5 °C at 760 mmHg
  • Flash Point:
  • 226.3 °C
  • Safety:
  • 24/25 Details

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CAS No.24758-49-4 Methanone,[4-(4-morpholinyl)phenyl]phenyl-Competitive Product

Supplier:Zhejiang Genebest Pharmaceutical Co.,Ltd. [ China (Mainland)]

Platinum
Supplier
ManufacturerISO 1385Integral
1385

Tel:0086-571-63532866

Address:No.1 Jinboshi Rd Lishan Town Fuyang City Zhejiang Province China

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CAS No.24758-49-4 Methanone,[4-(4-morpholinyl)phenyl]phenyl-

4-Morpholino-Benzophenone

Supplier:Anhui Charm Imp.&Exp.Co., Ltd [ China (Mainland)]

Platinum
Supplier
925Integral
925

Tel:86 551 5316260

Address:No. 211,XiangZhang Road,Hefei City,Anhui Province,China

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CAS No.24758-49-4 Methanone,[4-(4-morpholinyl)phenyl]phenyl-

6-MORPHOLINOBENZOPHENONE

Supplier:Norquay Technology Incorporated, U.S.A. [ United States]

540Integral
540

Tel:610 874 4330

Address:PO Box 468 Chester, PA 19016-0468 USA

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Reference

Substituted naphthopyrans and photochromic plastic articles containing or coated with these compounds
Substituted naphthopyrans and photochromic plastic articles containing or coated with these compounds. Kumar, Anil; Knowles, David B.; Van Gemert, Barry (Transitions Optical, Inc., USA). U.Some chemicals with cas registry numbers like 24758-49-4 are also used.S. US 5658500 A 19 Aug 1997, 15 pp. (English). (United States of America). CODEN: USXXAM. CLASS: ICM: C08K005-15. ICS: C07D311-78; C07D405-02; G02B005-23. NCL: 252586000. APPLICATION: US 1995-490188 14 Jun 1995. DOCUMENT TYPE: Patent CA Section: 41 (Dyes, Organic Pigments, Fluorescent Brighteners, and Photographic Sensitizers) Section cross-reference(s): 37, 74 Described are novel reversible photochromic 2H-naphtho[1,2-b]pyran compds., examples of which are compds. having certain substituents at the no. 5 carbon atom of the naphtho-portion of the naphthopyran and at the 2-position of the pyran ring. There are some commonly used reagents like 24758-49-4 in this article. Certain substituents may also be present at the no. 6, 7, 8, 9 or 10 carbon atoms of the naphtho portion of the naphthopyran. These substituted naphthopyrans exhibit acceptable fade rate, high activated intensity, and high coloration rate in plastics. Thus, reaction of 4-fluorobenzophenone with morpholine, reaction of the intermediate with Na acetylide, and reaction of the 2nd intermediate with Me 1,4-hydroxy-2-naphthoate gave 2-(4-morpholinophenyl)-6-hydroxy-5-methoxy-2-phenyl-2H-naphtho[1,2- b]pyran. ..
Substituted naphthopyrans and photochromic plastic articles containing or coated with these compounds
Substituted naphthopyrans and photochromic plastic articles containing or coated with these compounds. Kumar, Anil; Knowles, David B.; Van Gemert, Barry (Transitions Optical, Inc., USA). U.Some chemicals with cas registry numbers like 24758-49-4 are also used.S. US 5658500 A 19 Aug 1997, 15 pp. (English). (United States of America). CODEN: USXXAM. CLASS: ICM: C08K005-15. ICS: C07D311-78; C07D405-02; G02B005-23. NCL: 252586000. APPLICATION: US 1995-490188 14 Jun 1995. DOCUMENT TYPE: Patent CA Section: 41 (Dyes, Organic Pigments, Fluorescent Brighteners, and Photographic Sensitizers) Section cross-reference(s): 37, 74 Described are novel reversible photochromic 2H-naphtho[1,2-b]pyran compds., examples of which are compds. having certain substituents at the no. 5 carbon atom of the naphtho-portion of the naphthopyran and at the 2-position of the pyran ring. There are some commonly used reagents like 24758-49-4 in this article. Certain substituents may also be present at the no. 6, 7, 8, 9 or 10 carbon atoms of the naphtho portion of the naphthopyran. These substituted naphthopyrans exhibit acceptable fade rate, high activated intensity, and high coloration rate in plastics. Thus, reaction of 4-fluorobenzophenone with morpholine, reaction of the intermediate with Na acetylide, and reaction of the 2nd intermediate with Me 1,4-hydroxy-2-naphthoate gave 2-(4-morpholinophenyl)-6-hydroxy-5-methoxy-2-phenyl-2H-naphtho[1,2- b]pyran. ..
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