2-Methyl-1-pyrroline
2-Methyl-1-pyrroline Basic information
- Product Name:
- 2-Methyl-1-pyrroline
- Synonyms:
-
- 3,4-DIHYDRO-5-METHYL-2H-PYRROLE
- 2-METHYL-1-PYRROLINE
- 2-Methylpyrroline
- 2-Methyl-1-pyrroline 95%
- 2-Methyl-1-pyrroline≥ 99% (GC)
- 2-Methyl-4,5-dihydro-3H-pyrrole
- 5-Methyl-3,4-dihydro-2H-pyrrole
- 2-Methyl-1-pyrroline,98%
- CAS:
- 872-32-2
- MF:
- C5H9N
- MW:
- 83.13
- EINECS:
- 212-822-9
- Product Categories:
-
- Pyrrole&Pyrrolidine&Pyrroline
- Building Blocks
- Heterocyclic Building Blocks
- Pyrrolines
- Mol File:
- 872-32-2.mol
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2-Methyl-1-pyrroline Chemical Properties
- Boiling point:
- 104-105 °C(lit.)
- Density
- 0.878 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.444(lit.)
- Flash point:
- 51 °F
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- solubility
- Chloroform (Sparingly), Methanol (Sparingly)
- form
- Crystalline Powder and/or Chunks
- pka
- 8.41±0.20(Predicted)
- color
- White to pale yellow to beige
- Water Solubility
- soluble
- CAS DataBase Reference
- 872-32-2(CAS DataBase Reference)
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Safety Information
- Hazard Codes
- F,Xi
- Risk Statements
- 11-36/37/38-34-/11
- Safety Statements
- 16-26-33-45-36/37/39-/16
- RIDADR
- UN 1993 3/PG 2
- WGK Germany
- 3
- HazardClass
- 3
- PackingGroup
- II
- HS Code
- 29339900
MSDS
- Language:English Provider:2-Methyl-1-pyrroline
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
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2-Methyl-1-pyrroline Usage And Synthesis
Chemical Properties
clear colorless to yellow liquid
Uses
2-Methyl-1-pyrroline acts as monocyclic imine. It is a pharmaceutical intermediate.
Definition
ChEBI: A member of the class of pyrrolines that is 1-pyrroline substituted at position 2 by a methyl group.
General Description
2-Methyl-1-pyrroline, a monocyclic imine, is a pyrroline derivative. It is a five-membered heterocyclic compound having various biological and pharmacological applications. It is formed during the Rh(I) complexes (containing N,N-donor ligands and N,P-donor ligand) immobilized on glassy carbon electrode surfaces catalyzed intramolecular hydroamination of 4-pentyn-1-amine. It reacts with with 2-oxopropanal to afford acetyl-1-pyrroline (AP).
2-Methyl-1-pyrrolineSupplier
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