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4'-Aminobenzo-15-crown-5-ether

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4'-Aminobenzo-15-crown-5-ether Basic information

Product Name:
4'-Aminobenzo-15-crown-5-ether
Synonyms:
  • (BENZO-15-CROWN-5)-4'-YLAMINE
  • 2,3-(4'-AMINOBENZO)-1,4,7,10,13-PENTAOXACYCLOPENTADEC-2-ENE
  • 2,3-(4-AMINOBENZO)-1,4,7,10,13-PENTAOXACYCLOPENTADEC-2-ENE
  • 4'-AMINOBENZO-15-CROWN-5
  • 4'-AMINOBENZO-15-CROWN 5-ETHER
  • 2,3-(4'-Aminobenzo)-1,4,7,10,13-pentaxoacyclopentadec-2-ene
  • 4-AMINOBENZO-15-CROWN-5 PURUM,97%
  • 4''-AMINOBENZO-15-CROWN 5-ETHER95+%
CAS:
60835-71-4
MF:
C14H21NO5
MW:
283.32
Product Categories:
  • Crown Ethers
  • Functional Materials
  • Macrocycles for Host-Guest Chemistry
Mol File:
60835-71-4.mol
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4'-Aminobenzo-15-crown-5-ether Chemical Properties

Melting point:
76-78 °C(lit.)
Boiling point:
464.4±45.0 °C(Predicted)
Density 
1.118±0.06 g/cm3(Predicted)
pka
4.63±0.20(Predicted)
form 
powder to crystal
color 
White to Gray to Brown
BRN 
1587285
InChI
InChI=1S/C14H21NO5/c15-12-1-2-13-14(11-12)20-10-8-18-6-4-16-3-5-17-7-9-19-13/h1-2,11H,3-10,15H2
InChIKey
CQNGAZMLFIMLQN-UHFFFAOYSA-N
SMILES
O1C2=CC=C(N)C=C2OCCOCCOCCOCC1
CAS DataBase Reference
60835-71-4
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37
WGK Germany 
3
8-10
HS Code 
29329990

MSDS

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4'-Aminobenzo-15-crown-5-ether Usage And Synthesis

Chemical Properties

4'-Aminobenzo-15-crown-5-ether is a white to grey to brown powder to crystal in appearance, with a density of 1.1 g/cm3, a melting point of 76.0 ~ 80.0 °C, a boiling point of about 464.4° C, and is soluble in water (partially) and chloroform. Sensitive to light and air, store under inert gas.

Uses

4'-Aminobenzo-15-crown-5-ether is an organic heterocyclic compound that is a highly adaptable intermediate in the manufacture of a wide variety of organic compounds such as dyes and polymers. It is also used in the field of materials science and is an essential component in the development of a wide range of materials from nanomaterials to polymers. In scientific studies, the compound has shown inhibitory effects on other enzymes such as acetylcholinesterase and histone deacetylase. In addition, the compound has shown the ability to bind and activate specific receptors such as the 5-HT2A receptor.

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