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Detail of "1614-92-2"

  • CAS Number:
  • 1614-92-2
  • Name:
  • Piperidine,1-(1-cyclopenten-1-yl)-

  • Molecular Structure:
  • Formula:
  • C10H17N
  • Molecular Weight:
  • 151.25
  • Synonyms:
  • 1-(1-Cyclopenten-1-yl)piperidine;1-Piperidino-1-cyclopentene;1-Piperidinocyclopentene;1-(1-Cyclopentenyl)piperidine;
  • Density:
  • 1 g/cm3
  • Boiling Point:
  • 241.9 °C at 760 mmHg
  • Flash Point:
  • 91.4 °C

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CAS No.1614-92-2 Piperidine,1-(1-cyclopenten-1-yl)-

1-(Cyclopenten-1-yl)piperidine

Supplier:Synthon Chemicals GmbH & Co. KG [ Germany]

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Tel:+49 3494 636983

Address:Chemiepark Bitterfeld-Wolfen, Areal A, Werkstattstrasse 10

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CAS No.1614-92-2 Piperidine,1-(1-cyclopenten-1-yl)-

Supplier:CHEMOS GmbH [ Germany]

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Tel:+49 9402 9336 0

Address:Werner-von-Siemens Str. 3 D-93128 Regenstauf / Germany

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CAS No.1614-92-2 Piperidine,1-(1-cyclopenten-1-yl)-

Supplier:Wako Pure Chemical Industries, Ltd. [ Japan]

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Tel:+81 6 6203 3741

Address:1-2 Doshomachi 3-Chome, Chuo-ku, Osaka 540-8605, Japan

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Reference

Solid supported reactions and reagents
Solid supported reactions and reagents. Part 13. Envirocat Epz10 as a new catalyst for the synthesis of enamines without solvent. Bandgar, B.P.; Kulkani, Mahesh M. (Department of Chemistry, P.G. and Research Centre, R.B.N.B. College, Shrirampur 413 709, India). Indian Journal of Heterocyclic Chemistry, 6(2), 147-148 (English) 1996 Lucknow University, Dep. of Chemistry. CODEN: IJCHEI. 1614-92-2 and 7148-07-4 which are cas registry numbers of substances are two of reagents here. ISSN: 0971-1627. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) The synthesis of enamines from cycloalkanones and secondary cyclic amines has been carried out in good yields by using Envirocat EPZ10R as a new reusable heterogeneous catalyst. .
Fluoro-containing heterocycles: XIV
All Rights Reserved. Fluoro-containing heterocycles: XIV. Cyclic adducts of 6-fluoro-7-azidoquinoxaline and their transformation products. Mochul'skaya, N. N.; Nagibina, E. N.; Volchenkova, Yu. S.; Sidorova, L. P.; Charushin, V. N. (Ural State Technical University, Yekaterinburg 620219, Russia). Russian Journal of Organic Chemistry, 41(11), 1694-1701 (English) 2005 Pleiades Publishing, Inc. CODEN: RJOCEQ. ISSN: 1070-4280. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) The possibility of a structural modification of quinoxalines through 1,3-dipolar cycloaddn. of 7-azido-6-fluoroquinoxaline to norbornenes, enamines of cyclic ketones, and di-Me acetylenedicarboxylate was demonstrated. The stability of 1,2,3-triazoline adducts, e.There are some commonly used reagents with their cas registry numbers 1614-92-2 and 920034-18-0 in this article.g., I, was studied and the structure of the products of their mol. rearrangements was established. The cycloadduct of azide with cyclohexanone enamine underwent azapinacolone rearrangement involving a contraction of the cycloalkane ring by one member affording amidine of cyclopentanecarboxylic acid. The triazoline adduct of the azide with dicyclopentadiene as a result of the rearrangement afforded the corresponding aziridinoquinoxaline. .
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