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Detail of "1128-76-3"

  • CAS Number:
  • 1128-76-3
  • Name:
  • Benzoic acid,3-chloro-, ethyl ester

  • Molecular Structure:
  • Formula:
  • C9H9ClO2
  • Molecular Weight:
  • 184.62
  • Synonyms:
  • Benzoicacid, m-chloro-, ethyl ester (6CI,7CI,8CI);3-Chlorobenzoic acid ethyl ester;Ethyl 3-chlorobenzoate;Ethyl m-chlorobenzoate;NSC 67339;
  • EINECS:
  • 214-441-3
  • Density:
  • 1.185 g/cm3
  • Boiling Point:
  • 243 °C at 760 mmHg
  • Flash Point:
  • 115.2 °C
  • Safety:
  • 24/25 Details

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CAS No.1128-76-3 Benzoic acid,3-chloro-, ethyl ester

Assay:99%min  Appearance:standard  Package:UN DrumStorage:dry,cool  Transportation:by sea or ai...

Supplier:Zouping Mingxing Chemical Co.,Ltd. [ China (Mainland)]

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Manufacturer 2185Integral
2185

Tel:86-543-4350217

Address:428 Daixi Third Road Zouping County Shandong Province China

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CAS No.1128-76-3 Benzoic acid,3-chloro-, ethyl ester

Supplier:Shanghai Fchemicals Technology Co., Ltd [ China (Mainland)]

600Integral
600

Tel:021-36030322

Address:Room822, No.3, Wu Zhong Road, Shanghai, China

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Reference

Highly functionalized benzene syntheses by directed mono or multiple magnesiations with TMPMgCl×LiCl
All Rights Reserved. Highly functionalized benzene syntheses by directed mono or multiple magnesiations with TMPMgCl×LiCl. Lin, Wenwei; Baron, Oliver; Knochel, Paul (Department Chemie und Biochemie, Ludwig-Maximilians-Universitaet Muenchen, Munich 81377, Germany). Organic Letters, 8(24), 5673-5676 (English) 2006 American Chemical Society. CODEN: ORLEF7.In this article, certain chemicals are used. Some of their cas registry numbers are 1128-76-3 and 918402-93-4 ISSN: 1523-7060. DOCUMENT TYPE: Journal CA Section: 25 (Benzene, Its Derivatives, and Condensed Benzenoid Compounds) Section cross-reference(s): 29 The direct magnesiation of highly functionalized aroms. bearing an ester, a nitrile, or a ketone can be readily performed by using an OBoc as a directing group and TMPMgCl×LiCl as a base. It allowed, for example, the prepn. of a meta-magnesiated benzophenone in >95%. After quenching, highly functionalized and substituted benzenes were obtained. .
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