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Cyclohexylhydrazine hydrochloride

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Cyclohexylhydrazine hydrochloride Basic information

Product Name:
Cyclohexylhydrazine hydrochloride
Synonyms:
  • CYCLOHEXYLHYDRAZINE HYDROCHLORIDE
  • 1-CYCLOHEXYLHYDRAZINE HYDROCHLORIDE
  • CyclohexylhydrazineHCl
  • Hydrazinocyclohexane hydrochloride
  • Hydrazine, cyclohexyl-,hydrochloride (1:1)
  • Cyclohexylhydrazine hydrochloride 98%
  • Cyclohexylhydrazine hydrochloride≥ 98%(Titration)
  • Cyclohexylhydrazine monohydrochloride
CAS:
24214-73-1
MF:
C6H15ClN2
MW:
150.65
Product Categories:
  • Hydrazines
  • Nitrogen Compounds
  • Organic Building Blocks
Mol File:
24214-73-1.mol
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Cyclohexylhydrazine hydrochloride Chemical Properties

Melting point:
110-114 °C(lit.)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
Crystalline Powder
color 
White
Water Solubility 
almost transparency
InChI
InChI=1S/C6H14N2.ClH/c7-8-6-4-2-1-3-5-6;/h6,8H,1-5,7H2;1H
InChIKey
JZRHODNPRNTXKO-UHFFFAOYSA-N
SMILES
C1(NN)CCCCC1.Cl
CAS DataBase Reference
24214-73-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
26-36/37/39-45
RIDADR 
UN 3263 8/PG 2
WGK Germany 
3
HazardClass 
8
PackingGroup 
HS Code 
29280000

MSDS

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Cyclohexylhydrazine hydrochloride Usage And Synthesis

Chemical Properties

White to light yellow powder,crystals or

Synthesis

60295-21-8

24214-73-1

GENERAL METHOD: tert-Butyl 2-cyclohexylhydrazine-1-carboxylate (1.9 g, 8.87 mmol) was dissolved in dioxane and to this solution was added a dioxane solution (20 mL) of 4 M HCl. The reaction mixture was heated to reflux and stirred overnight. Upon completion of the reaction, it was cooled to room temperature, the precipitated white precipitate was collected by filtration, washed with a small amount of cold dioxane and dried to give cyclohexylhydrazine hydrochloride (1.8 g, yield: >100%) as a white solid.

References

[1] Patent: WO2016/123392, 2016, A2. Location in patent: Paragraph 00476
[2] Patent: WO2014/82598, 2014, A1. Location in patent: Paragraph 0419
[3] Journal of Organic Chemistry, 1981, vol. 46, # 26, p. 5413 - 5414
[4] Patent: WO2005/40169, 2005, A2. Location in patent: Page/Page column 150

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