20271-33-4 Usage
Description
ETHYL 5-AMINO-1-BENZYL-1H-1,2,3-TRIAZOLE-4-CARBOXYLATE is a chemical compound with the molecular formula C14H14N4O2. It is a derivative of 1,2,3-triazole and contains an amino group, a benzyl group, and a carboxylic acid ester group. ETHYL 5-AMINO-1-BENZYL-1H-1,2,3-TRIAZOLE-4-CARBOXYLATE is commonly used in organic synthesis and medicinal chemistry as a building block for the synthesis of various pharmaceutical drugs and biologically active molecules. It has potential applications in the development of new drugs for the treatment of various diseases and medical conditions. As a chemical, it is important to handle and use ETHYL 5-AMINO-1-BENZYL-1H-1,2,3-TRIAZOLE-4-CARBOXYLATE with care and caution due to its potential hazards and reactivity.
Uses
Used in Pharmaceutical Industry:
ETHYL 5-AMINO-1-BENZYL-1H-1,2,3-TRIAZOLE-4-CARBOXYLATE is used as a building block for the synthesis of various pharmaceutical drugs and biologically active molecules. Its unique structure and functional groups make it a valuable component in the development of new drugs for the treatment of various diseases and medical conditions.
Used in Organic Synthesis:
ETHYL 5-AMINO-1-BENZYL-1H-1,2,3-TRIAZOLE-4-CARBOXYLATE is used as a key intermediate in organic synthesis. Its versatile structure allows for the formation of a wide range of chemical compounds, making it a valuable tool in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
ETHYL 5-AMINO-1-BENZYL-1H-1,2,3-TRIAZOLE-4-CARBOXYLATE is used as a starting material in medicinal chemistry for the development of new drugs and therapeutic agents. Its potential applications in drug discovery make it an important compound in the field of medicinal chemistry.
Used in Research and Development:
ETHYL 5-AMINO-1-BENZYL-1H-1,2,3-TRIAZOLE-4-CARBOXYLATE is used in research and development for the exploration of its potential applications in various fields, including pharmaceuticals, organic synthesis, and medicinal chemistry. Its unique properties and reactivity make it an interesting subject for scientific investigation and innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 20271-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,7 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20271-33:
(7*2)+(6*0)+(5*2)+(4*7)+(3*1)+(2*3)+(1*3)=64
64 % 10 = 4
So 20271-33-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H14N4O2/c1-2-18-12(17)10-11(13)16(15-14-10)8-9-6-4-3-5-7-9/h3-7H,2,8,13H2,1H3
20271-33-4Relevant articles and documents
Ruthenium-catalyzed synthesis of 5-amino-1,2,3-triazole-4-carboxylates for triazole-based scaffolds: Beyond the Dimroth rearrangement
Ferrini, Serena,Chandanshive, Jay Zumbar,Lena, Stefano,Comes Franchini, Mauro,Giannini, Giuseppe,Tafi, Andrea,Taddei, Maurizio
, p. 2562 - 2572 (2015/03/18)
The 5-amino-1,2,3-triazole-4-carboxylic acid is a suitable molecule for the preparation of collections of peptidomimetics or biologically active compounds based on the triazole scaffold. However, its chemistry may be influenced by the possibility of under
A MODIFIED SCHEME FOR THE SYNTHESIS OF 1-BENZYL-4,5-DIAMINO-1,2,3-TRIAZOLE
Erashko, V. I.,El'yanova, B. S.,Baryshnikov, A. T.,Zubanova, N. I.,Tishaninova, A. A.
, p. 2440 - 2441 (2007/10/02)
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