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Catalog Number:
41454
CAS Number:
7202-43-9
(R)-(-)-Tetrahydrofurfurylamine
Purity:
≥ 98.5% (GC)
Synonym(s):
(R)-2-(Aminomethyl)tetrahydrofuran
Hazmat
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Product Information
Synonyms
(R)-2-(Aminomethyl)tetrahydrofuran
CAS Number
7202-43-9
Purity
≥ 98.5% (GC)
Molecular Formula
C5H11NO
Molecular Weight
0
MDL Number
MFCD00192476
PubChem ID
253298
Density
0.98 g/mL at 25 °C (Lit.)
Appearance
Colorless to pale yellow liquid
Boiling Point
55 °C / 18 mmHg (Lit.)
Refractive Index
n20D 1.45 (Lit.)
Optical Rotation
[á]20/D = −12 ° (C = 2 in Chloroform)
Conditions
Store at 2 - 8 °C
General Information
Synonyms
(R)-2-(Aminomethyl)tetrahydrofuran
CAS Number
7202-43-9
Purity
≥ 98.5% (GC)
Molecular Formula
C5H11NO
Molecular Weight
0
MDL Number
MFCD00192476
PubChem ID
253298
Density
0.98 g/mL at 25 °C (Lit.)
Appearance
Colorless to pale yellow liquid
Boiling Point
55 °C / 18 mmHg (Lit.)
Refractive Index
n20D 1.45 (Lit.)
Optical Rotation
[á]20/D = −12 ° (C = 2 in Chloroform)
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R)-(-)-Tetrahydrofurfurylamine is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly in the creation of drugs that target neurological disorders.
  • Agrochemical Formulations: It is used in the formulation of agrochemicals, enhancing the effectiveness of pesticides and herbicides by improving their solubility and absorption in plants.
  • Polymer Production: This chemical acts as a monomer in the production of biodegradable polymers, contributing to sustainable materials that reduce environmental impact.
  • Flavor and Fragrance Industry: It is employed as an intermediate in the synthesis of flavoring agents and fragrances, providing unique aromatic properties that enhance consumer products.
  • Research in Organic Chemistry: The compound is a valuable reagent in organic synthesis, facilitating various chemical reactions and enabling researchers to explore new synthetic pathways.

Citations