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Detail of "2981-10-4"

  • MSDS Download
  • CAS Number:
  • 2981-10-4
  • Name:
  • Piperidine,1-(1-cyclohexen-1-yl)-

  • Superlist Name:
  • 1-(1-Piperidino)cyclohexene
  • Molecular Structure:
  • Formula:
  • C11H19 N
  • Molecular Weight:
  • 165.27
  • Synonyms:
  • 1-(1-Cyclohexen-1-yl)piperidine;1-(Cyclohex-1-enyl)piperidine;1-Piperidino-1-cyclohexene;1-Piperidinocyclohexene;1-Piperidinylcyclohexene;N-(1-Cyclohexen-1-yl)piperidine;N-(1-Cyclohexenyl)piperidine;
  • Density:
  • 0.978g/cm3
  • Boiling Point:
  • 262.2oCat760mmHg
  • Flash Point:
  • 102.8oC
  • Appearance:
  • Clear yellow liquid
  • Risk Codes:
  • 22-36/38
  • Safety:
  • 26-36/37/39 Details

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CAS No.2981-10-4 1-(1-Piperidino)cyclohexene

1-(1-Piperidino)cyclohexene

Supplier:Hangzhou Sage Chemical Co.,Ltd [ China (Mainland)]

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CAS No.2981-10-4 1-(1-Piperidino)cyclohexene

Assay:99%

Supplier:Wuhan Pharma Chemical Co., Ltd. [ China (Mainland)]

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Address:Wuchang, Wuhan

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CAS No.2981-10-4 1-(1-Piperidino)cyclohexene

1-(Cyclohexen-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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Reference

1-Piperidinocyclohexanecarbonitrile, a toxic precursor of phencyclidine
1-Piperidinocyclohexanecarbonitrile, a toxic precursor of phencyclidine.Some chemicals with cas registry numbers like 2981-10-4 and 1934-67-4 are also used. Bailey, Keith; Chow, Alan Y. K.; Downie, Robert H.; Pike, Richard K. (Health Protect. Branch, Drug Res. Lab., Ottawa, Ont., Can.). J. Pharm. Pharmacol., 28(9), 713-14 (English) 1976. CODEN: JPPMAB. DOCUMENT TYPE: Journal CA Section: 4 (Toxicology) Spectroscopic and chromatog. studies of phencyclidine (I) [77-10-1] samples indicated the presence of 1-piperidinocyclohexanecarbonitrile (II) [3867-15-0]. The LD50 of I-HCl [956-90-1], II, II-HCl [1934-67-4], and 1-cyclohexenylpiperidine [2981-10-4] in mice were 76.5, 133.0, 59.5, and 1272.7 mg/kg resp. NaNO2 and Na2S2O3 individually gave some protection against the lethal effects of II-HCl and pretreatment with NaNO2 + Na2S2O3 gave increased protection against II and II-HCl, but neither salt protected against I, suggesting that CN- may be a metabolite of II and II-HCl in mice. II-HCl (45, 50, and 55 mg/kg) did not appear to be either hepatotoxic or nephrotoxic in mice. .
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