14496-33-4 Usage
General Description
ETHYL-FURAN-2-YLMETHYL-AMINE is a chemical compound that contains an ethyl group attached to a furan ring with a 2-ylmethylamine side chain. It is commonly used in organic synthesis and chemical research, and it has potential applications in the pharmaceutical industry. ETHYL-FURAN-2-YLMETHYL-AMINE is also known for its unique odor, which has been described as sweet and nutty. In addition, it has been studied for its potential biological activities and medicinal properties, including its potential as an anti-inflammatory and analgesic agent.ETHYL-FURAN-2-YLMETHYL-AMINE is a chemical compound that contains an ethyl group attached to a furan ring with a 2-ylmethylamine side chain. It is commonly used in organic synthesis and chemical research, and it has potential applications in the pharmaceutical industry. ETHYL-FURAN-2-YLMETHYL-AMINE is also known for its unique odor, which has been described as sweet and nutty. In addition, it has been studied for its potential biological activities and medicinal properties, including its potential as an anti-inflammatory and analgesic agent.
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 articles and documents
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Zanetti,Bashour
, p. 3133 (1939)
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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.