13670-24-1 Usage
Heterocyclic compound
1H-Imidazole, 2-ethyl-4,5-dihydro-1-phenylis a compound that contains a ring structure with one nitrogen atom among its members.
5-membered ring structure
The compound has a closed ring structure consisting of 5 atoms.
Phenyl group
A carbon atom in position 1 of the compound is attached to a phenyl group, which is a benzene ring with a hydrogen atom removed.
Ethyl group
The nitrogen atom in position 2 of the compound is attached to an ethyl group, which is a two-carbon chain with a hydrogen atom attached to each carbon.
Building block for synthesis
1H-Imidazole, 2-ethyl-4,5-dihydro-1-phenylis commonly used in the pharmaceutical and agrochemical industries as a starting material for the synthesis of various drugs and biologically active compounds.
Antifungal and antiparasitic activity
The compound has the ability to inhibit the growth of fungi and parasites, making it a potential candidate for the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 13670-24-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,7 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13670-24:
(7*1)+(6*3)+(5*6)+(4*7)+(3*0)+(2*2)+(1*4)=91
91 % 10 = 1
So 13670-24-1 is a valid CAS Registry Number.
13670-24-1Relevant academic research and scientific papers
Electrophilically activated nitroalkanes in reaction with aliphatic diamines en route to imidazolines
Aksenov, Alexander V.,Aksenov, Nicolai A.,Arutiunov, Nikolai A.,Malyuga, Vladimir V.,Ovcharov, Sergey N.,Rubin, Michael
, p. 39458 - 39465 (2019/12/14)
A novel synthetic methodology for the assembly of imidazolines via an unusual reaction between nitroalkanes and aliphatic 1,2-diamines in the presence of phosphorous acid is described. In contrast to the related highly efficient preparation of benzimidazoles from aromatic amines, this process represents a major synthetic challenge and for a long time was elusive. Analysis of the method limitations is provided.
One-pot triflic anhydride-mediated synthesis of 1,2-disubstituted 2-imidazolines from N-(2-haloethyl)amides and amines
Ellsworth, Alyssa A.,Magyar, Christina L.,Hubbell, Grace E.,Theisen, Chelsea C.,Holmes, Daniel,Mosey, R. Adam
, p. 6380 - 6389 (2016/09/23)
A one-pot synthesis of 1,2-disubstituted 2-imidazolines from N-(2-haloethyl)amides has been developed. The reaction affords high yields of diverse 1,2-disubstituted 2-imidazolines from triflic anhydride-mediated dehydration of amides followed by installat
