ethyl 1H-1,2,3-triazole-4-carboxylate

Base Information

Chemical Name:ethyl 1H-1,2,3-triazole-4-carboxylate
CAS No.:40594-98-7
Molecular Formula:C5H7 N3 O2
Molecular Weight:141.129
Hs Code.:2933990090
European Community (EC) Number:832-095-7
DSSTox Substance ID:DTXSID30423546
Nikkaji Number:J1.006.153I
Wikidata:Q72477498
Mol file:40594-98-7.mol

Synonyms:ethyl 1H-1,2,3-triazole-4-carboxylate;40594-98-7;ethyl 2H-1,2,3-triazole-4-carboxylate;1084802-21-0;ethyl 1H-1,2,3-triazole-5-carboxylate;ethyl 2H-triazole-4-carboxylate;1H-1,2,3-Triazole-4-carboxylic acid, ethyl ester;ethyl 1,2,3-triazole-4-carboxylate;MFCD08669518;1H-1,2,3-triazole-4-carboxylic acid ethyl ester;1H-1,2,3-Triazole-5-carboxylic Acid Ethyl Ester;SCHEMBL561752;ethyl 1H-triazole-4-carboxylate;DTXSID30423546;BMGCDMZWMQQHMI-UHFFFAOYSA-N;5-ethoxycarbonyl-1,2,3-triazole;MFCD27959308;4-ethoxycarbonyl-2h-1,2,3-triazole;AKOS007930815;AKOS027404018;Quinoline-5-carboxylic acid ethyl ester;AM803858;DS-16918;SY111481;CS-0037024;FT-0653257;FT-0768744;EN300-136557;O11755;Z1118834497

Suppliers and Price of ethyl 1H-1,2,3-triazole-4-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
1H-1,2,3-Triazole-5-carboxylicAcidEthylEster
250mg
$ 415.00

Medical Isotopes, Inc.
1H-1,2,3-Triazole-5-carboxylicAcidEthylEster
250 mg
$ 875.00

Medical Isotopes, Inc.
1H-1,2,3-Triazole-5-carboxylicAcidEthylEster
1 g
$ 2125.00

Matrix Scientific
Ethyl 1H-1,2,3-triazole-4-carboxylate
10g
$ 2324.00

Matrix Scientific
Ethyl 1H-1,2,3-triazole-4-carboxylate
5g
$ 1537.00

Matrix Scientific
Ethyl 1H-1,2,3-triazole-4-carboxylate
1g
$ 466.00

Crysdot
Ethyl1H-1,2,3-triazole-4-carboxylate 96%
5g
$ 306.00

ChemScene
Ethyl1H-1,2,3-triazole-5-carboxylate 99.07%
5g
$ 321.00

ChemScene
Ethyl1H-1,2,3-triazole-5-carboxylate 99.07%
1g
$ 90.00

Ark Pharm
Ethyl1H-1,2,3-triazole-4-carboxylate 98+%
250mg
$ 37.00

Total 27 raw suppliers

Chemical Property of ethyl 1H-1,2,3-triazole-4-carboxylate

Chemical Property:

Vapor Pressure:0.00293mmHg at 25°C
Melting Point:102-104 °C
Boiling Point:284.7°C at 760 mmHg
PKA:6.94±0.70(Predicted)
Flash Point:126°C
PSA：67.87000
Density:1.299g/cm³
LogP:-0.01860
Storage Temp.:under inert gas (nitrogen or Argon) at 2-8°C
XLogP3:0.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:141.053826475
Heavy Atom Count:10
Complexity:128

Purity/Quality:

97% ^*data from raw suppliers

1H-1,2,3-Triazole-5-carboxylicAcidEthylEster ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1=NNN=C1
Uses 1H-1,2,3-Triazole-5-carboxylic Acid Ethyl Ester is used in the synthesis potent inhibitors of bacterial β-lactamase.

Technology Process of ethyl 1H-1,2,3-triazole-4-carboxylate

There total 1 articles about ethyl 1H-1,2,3-triazole-4-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 73.0%

: 941-55-9
4-toluenesulfonyl azide

: 87051-40-9
butyl β-methylaminoacrylate

: 40594-98-7
ethyl 1H-1,2,3-triazole-4-carboxylate

: 1907-65-9
N-butyl-4-toluenesulfonamide

: C₁₂H₁₈N₂O₂S

Guidance literature:: In acetonitrile; at 20 ℃;
DOI:10.1039/d1ra00772f

Reference yield: 88.0%

: 100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6
styrene

: 40594-98-7
ethyl 1H-1,2,3-triazole-4-carboxylate

: ethyl 1-(2-hydroxy-2-phenylethyl)-1H-1,2,3-triazole-4-carboxylate

Guidance literature:: styrene; With N-Bromosuccinimide; In dimethyl sulfoxide; at 0 - 25 ℃; for 8h;

ethyl 1H-1,2,3-triazole-4-carboxylate; With sodium tetrahydroborate; In dimethyl sulfoxide; at 0 - 25 ℃; for 1h; regioselective reaction;
DOI:10.1021/acs.orglett.5b03540