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ChemicalBook >  Product Catalog >  Flavors and fragrances >  Synthetic fragrances >  Oxygen-containing heterocyclic compounds >  Thiazole, thiophene, and pyridine >  2,4-Dimethyl-3-ethyl-1H-pyrrole

2,4-Dimethyl-3-ethyl-1H-pyrrole

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2,4-Dimethyl-3-ethyl-1H-pyrrole Basic information

Product Name:
2,4-Dimethyl-3-ethyl-1H-pyrrole
Synonyms:
  • 1H-Pyrrole, 3-ethyl-2,4-diMethyl-
  • Cryptopyrrole Kryptopyrrole
  • 3-Ethyl-2,4-dimethylpyrole
  • TIMTEC-BB SBB004274
  • Haemopyrrole C
  • 2,4-Dimethyl-3-ethylpyrrole,96%
  • KRYPTOPYRROLE
  • CRYPTOPYRROLE
CAS:
517-22-6
MF:
C8H13N
MW:
123.2
EINECS:
208-234-7
Product Categories:
  • Pharmaceutial intermediates
Mol File:
517-22-6.mol
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2,4-Dimethyl-3-ethyl-1H-pyrrole Chemical Properties

Melting point:
63.75°C (estimate)
Boiling point:
197 °C/710 mmHg (lit.)
Density 
0.913 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.496(lit.)
Flash point:
161 °F
storage temp. 
2-8°C
solubility 
Chloroform (Soluble), Methanol (Slightly)
pka
18.33±0.50(Predicted)
form 
Liquid
color 
Clear yellow to red-brown
Specific Gravity
0.913
BRN 
107089
CAS DataBase Reference
517-22-6(CAS DataBase Reference)
NIST Chemistry Reference
1H-Pyrrole, 3-ethyl-2,4-dimethyl-(517-22-6)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
RTECS 
UX9629500
HS Code 
29339900

MSDS

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2,4-Dimethyl-3-ethyl-1H-pyrrole Usage And Synthesis

Chemical Properties

clear yellow to red-brown liquid

Uses

3-Ethyl-2,4-dimethyl-1H-pyrrole is a important diagnostic compound for pyrrole disorder or pyroluria, an abnormality in biochemistry resulting in overproduction of pyrrole molecules and resulting in improper hemoglobin synthesis.

Uses

3-Ethyl-2,4-dimethylpyrrole can be used as a substrate for the synthesis of:

  • Boradiazaindacene (BODIPY dyes) units as a building block for the fabrication of energy transfer cassettes.
  • Meso-benzyl and meso-alkyl dipyrrins salts by treating with corresponding acid chloride.
  • 2,5-Bis[3,5-dimethyl-4-ethylpyrrol-2-yl]cyclohexadiene-1,4-dione by reacting with 1,4-benzoquinone.

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