14496-33-4 Usage
Uses
Used in Organic Synthesis:
ETHYL-FURAN-2-YLMETHYL-AMINE is used as a building block in organic synthesis for creating a variety of complex organic molecules due to its unique structure and reactivity.
Used in Chemical Research:
In the field of chemical research, ETHYL-FURAN-2-YLMETHYL-AMINE serves as a valuable compound for studying reaction mechanisms and exploring new synthetic pathways.
Used in Pharmaceutical Industry:
ETHYL-FURAN-2-YLMETHYL-AMINE is used as a precursor in the development of pharmaceuticals, leveraging its potential biological activities and medicinal properties.
Used in Anti-inflammatory Applications:
ETHYL-FURAN-2-YLMETHYL-AMINE is used as an anti-inflammatory agent for its potential to reduce inflammation, offering a new avenue for the treatment of inflammatory conditions.
Used in Analgesic Applications:
As an analgesic agent, ETHYL-FURAN-2-YLMETHYL-AMINE is utilized for its pain-relieving properties, providing an alternative for managing various types of pain.
Check Digit Verification of cas no
The CAS Registry Mumber 14496-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,9 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14496-33:
(7*1)+(6*4)+(5*4)+(4*9)+(3*6)+(2*3)+(1*3)=114
114 % 10 = 4
So 14496-33-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO/c1-2-8-6-7-4-3-5-9-7/h3-5,8H,2,6H2,1H3
14496-33-4Relevant academic research and scientific papers
Kozintsev, S. I.,Basalaeva, L. I.,Gladkikh, L. V.,Kozlov, N. S.
, p. 19 - 21 (1988)
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.
Deoxygenative hydroboration of primary, secondary, and tertiary amides: Catalyst-free synthesis of various substituted amines
An, Duk Keun,Jaladi, Ashok Kumar,Kim, Hyun Tae,Yi, Jaeeun
, (2021/11/17)
Transformation of relatively less reactive functional groups under catalyst-free conditions is an interesting aspect and requires a typical protocol. Herein, we report the synthesis of various primary, secondary, and tertiary amines through hydroboration of amides using pinacolborane under catalyst-free and solvent-free conditions. The deoxygenative hydroboration of primary and secondary amides proceeded with excellent conversions. The comparatively less reactive tertiary amides were also converted to the corresponding N,N-diamines in moderate yields under catalyst-free conditions, although alcohols were obtained as a minor product.
