1260877-21-1 Usage
Chemical class
Imidazole carboxylic acid derivatives It belongs to a group of compounds derived from imidazole, which is a heterocyclic aromatic organic compound.
Structure
2-(4-Bromophenyl)-5-methyl-3H-imidazole-4-carboxylic acid ethyl ester The compound is characterized by a 4-bromophenyl group at position 2, a methyl group at position 5, and an ethyl ester group attached to the imidazole ring.
Functional groups
Ester, Bromine, Methyl The compound contains an ester group (-COO-), a bromine atom (-Br), and a methyl group (-CH3) as its main functional groups.
Use in organic synthesis
As an intermediate This compound serves as a valuable intermediate in the production of various organic compounds due to its properties and reactivity.
Pharmaceutical applications
Potential drug development 2-(4-Bromophenyl)-5-methyl-3H-imidazole-4-carboxylic acid ethyl ester is used in pharmaceutical research and has potential applications in the development of new drugs and pharmaceutical products.
Check Digit Verification of cas no
The CAS Registry Mumber 1260877-21-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,8,7 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1260877-21:
(9*1)+(8*2)+(7*6)+(6*0)+(5*8)+(4*7)+(3*7)+(2*2)+(1*1)=161
161 % 10 = 1
So 1260877-21-1 is a valid CAS Registry Number.
1260877-21-1Relevant articles and documents
Synthesis of di- and tri-substituted imidazole-4-carboxylates via PBu3-mediated [3+2] cycloaddition
Hsu, Mei-Yuan,Dietrich, Justin,Hulme, Christopher,Shaw, Arthur Y.
, p. 1538 - 1542 (2013/05/21)
Some new di- and trisubstituted imidazole-4-carboxylates were prepared from amidoacetic acids 3 in the present report. The key step to establish such imidazole- 4-carboxylates stemmed from the PBu3-mediated [3+2] cycloaddition between in situ-generated Δ2-oxazolinone 4 and ethyl cyanoformate6. Our results indicated that trisubstituted imidazoles 7-20 were afforded in better yields than those of disubstituted imidazoles 21-27. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications1 to view the free supplemental file. Copyright Taylor & Francis Group, LLC.
