7179-87-5 Usage
Uses
Used in Organic Synthesis:
PROPYL-(TETRAHYDRO-FURAN-2-YLMETHYL)-AMINE is used as a building block in organic synthesis for its ability to facilitate the creation of diverse chemical compounds.
Used in Pharmaceutical Research:
In pharmaceutical research, PROPYL-(TETRAHYDRO-FURAN-2-YLMETHYL)-AMINE is utilized as a key component in the development of new drugs and pharmaceuticals, leveraging its chemical properties to enhance medicinal formulations.
Used in Medicinal Chemistry:
PROPYL-(TETRAHYDRO-FURAN-2-YLMETHYL)-AMINE is employed in medicinal chemistry for its potential to contribute to the discovery and design of innovative therapeutic agents.
Used in Polymer Production:
PROPYL-(TETRAHYDRO-FURAN-2-YLMETHYL)-AMINE may also be used in the production of certain polymers, where its unique structure can influence the properties of the resulting materials.
Used in Industrial Material Production:
PROPYL-(TETRAHYDRO-FURAN-2-YLMETHYL)-AMINE finds applications in the creation of various industrial materials, potentially improving their performance and functionality.
Check Digit Verification of cas no
The CAS Registry Mumber 7179-87-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,7 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7179-87:
(6*7)+(5*1)+(4*7)+(3*9)+(2*8)+(1*7)=125
125 % 10 = 5
So 7179-87-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H17NO/c1-2-5-9-7-8-4-3-6-10-8/h8-9H,2-7H2,1H3
7179-87-5Relevant academic research and scientific papers
Catalytic Hydroamination of Furfuryl and Tetrahydrofurfuryl Alcohols with Nitriles
Kozintsev, S. I.,Basalaeva, L. I.,Gladkikh, L. V.,Kozlov, N. S.
, p. 19 - 21 (2007/10/02)
Reaction of furfuryl and tetrahydrofurfuryl alcohols with nitriles over copper oxide catalysts under a hydrogen pressure of 15 atm at a temperature of 230 deg C gives N-alkylfurfuryl- (yield 46-50percent) and N-alkyltetrahydrofurfurylamines (49-53percent), and N-alkylpiperidines (28-41percent).A reaction mechanism is proposed.
