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1-Pyrrolidino-1-cyclohexene

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Products Intro: Product Name:1-Pyrrolidino-1-cyclohexene
CAS:1125-99-1
Purity:99% Package:1KG;100USD|1000KG;1USD
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CAS:1125-99-1
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CAS:1125-99-1
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CAS:1125-99-1
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Products Intro: Product Name:N-(cyclohex-1-en-1-yl)pyrrolidine
CAS:1125-99-1

1-Pyrrolidino-1-cyclohexene manufacturers

  • 1-Pyrrolidino-1-cyclohexene
  • 1-Pyrrolidino-1-cyclohexene pictures
  • $100.00 / 1KG
  • 2025-09-25
  • CAS:1125-99-1
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: g-kg-tons, free sample is available
1-Pyrrolidino-1-cyclohexene Basic information
Product Name:1-Pyrrolidino-1-cyclohexene
Synonyms:Cyclohexanone pyrrolidine enamine;N-(1-Cyclohexenyl)pyrrolidine;N-Pyrrolidino-1-cyclohexene;N-(1-CYCLOHEXEN-1-YL)-PYRROLIDIN;N-(1-CYCLOHEXEN-1-YL)PYRROLIDINE;1-PYRROLIDINO-1-CYCLOHEXENE;1-PYRROLIDINO-2-CYCLOHEXENE;1-(1-PYRROLIDINO)CYCLOHEXENE
CAS:1125-99-1
MF:C10H17N
MW:151.25
EINECS:214-414-6
Product Categories:API intermediates;Miscellaneous
Mol File:1125-99-1.mol
1-Pyrrolidino-1-cyclohexene Structure
1-Pyrrolidino-1-cyclohexene Chemical Properties
Melting point 113 °C
Boiling point 114-115 °C/15 mmHg (lit.)
density 0.94 g/mL at 25 °C (lit.)
refractive index n20/D 1.5217(lit.)
Fp 103 °F
storage temp. 2-8°C
pka8.91±0.20(Predicted)
form Liquid
color Clear light yellow
Sensitive Air Sensitive
BRN 114797
CAS DataBase Reference1125-99-1(CAS DataBase Reference)
NIST Chemistry ReferencePyrrolidine, 1-(1-cyclohexen-1-yl)-(1125-99-1)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 10-36/37/38-20/21/22
Safety Statements 16-26-36/37/39
RIDADR UN 1993 3/PG 3
WGK Germany 3
HazardClass 3
PackingGroup III
HS Code 29339980
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
1-Pyrrolidino-1-cyclohexene Usage And Synthesis
Chemical Propertiesclear light yellow liquid
Uses1-Pyrrolidino-1-cyclohexene is a cyclic enamine that is used as an electron-rich dienophile in synthetic reactions.
Synthesis Reference(s)Chemical and Pharmaceutical Bulletin, 16, p. 1466, 1968 DOI: 10.1248/cpb.16.1466
Reactivity ProfileThe enamine nitrogen and its β-carbon atom are nucleophilic, undergoing substitution or conjugate addition; they can take part in 1,2- or 1,4-cycloadditions; iminium salts act as electrophiles.
Synthesis The most commonly used preparation method for these enamines is the acid-catalyzed condensation of a secondary amine with cyclohexanone. An example is the reaction of Pyrrolidine with cyclohexanone (eq 1). Using a preformed Titanium(IV) Chloride-amine complex with cyclohexanone greatly decreases the reaction time while maintaining high yields. This technique is also effective with functionalized cyclohexanones. When unsymmetrical tin(II) amides are allowed to react with cyclohexanone, good yields of enamines result.
1-Pyrrolidino-1-cyclohexene
PrecautionsReadily reacts with water or atmospheric oxygen; should be stored under dry nitrogen.
Tag:1-Pyrrolidino-1-cyclohexene(1125-99-1) Related Product Information
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