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Details

Stereochemistry ACHIRAL
Molecular Formula C2H4N4
Molecular Weight 84.08
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-AMINO-1,2,4-TRIAZOLE

SMILES

NN1C=NN=C1

InChI

InChIKey=FMCUPJKTGNBGEC-UHFFFAOYSA-N
InChI=1S/C2H4N4/c3-6-1-4-5-2-6/h1-2H,3H2

HIDE SMILES / InChI

Molecular Formula C2H4N4
Molecular Weight 84.08
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
4-Amino-1H-1,2,4-triazol-1-ium nitrate.
2010-12-04
Spin crossover-macromolecule composite nano film material.
2010-07-28
Synthesis and explosive properties of copper(II) chlorate(VII) coordination polymer with 4-amino-1,2,4-triazole bridging ligand.
2010-05-15
Mechanism for optical switching of the spin crossover [Fe(NH(2)-trz)(3)](Br)(2).3H(2)O compound at room temperature.
2010-03-28
Multiple signals converge on a differentiation MAPK pathway.
2010-03-19
(E)-N-Benzyl-idene-4H-1,2,4-triazol-4-amine.
2010-02-06
6-Azahemiporphycene: a new member of the porphyrinoid family.
2009-11-02
[Synthesis, characterization and fluorescence of Zn3 (NCS)6 (L1)6 (NO3)2 and Ni3(NCS)6(L2)6(NO3)2].
2009-10
[Synthesis and spectra of transition metals complexes RE3L6(NO3)6(H2O)2].
2009-09
Poly[[diaqua-{N-[1-(3-pyrid-yl)ethyl-idene]-4H-1,2,4-triazol-4-amine}zinc(II)] bis-(perchlorate)].
2009-04-10
6-azahemiporphycene: a further example of corrole metamorphosis.
2009-03-28
Construction of a dinuclear silver(I) coordination complex with a Schiff base containing 4-amino-1,2,4-triazole ligands.
2009-02-18
Synthesis, IR, UV/vis-, (1)H NMR and DFT study of chelatophore functionalized 1,3-benzoxazinone spiropyrans.
2008-12-01
Nanoparticles of iron(II) spin-crossover.
2008-09-28
4-Amino-3,5-dimethyl-4H1-,2,4-triazole-water (2/3).
2008-09-06
4-[4-(Diethyl-amino)benzyl-ideneamino]-4H-1,2,4-triazole.
2008-05-03
Structure-activity relationships for NAMI-A-type complexes (HL)[trans-RuCl4L(S-dmso)ruthenate(III)] (L = imidazole, indazole, 1,2,4-triazole, 4-amino-1,2,4-triazole, and 1-methyl-1,2,4-triazole): aquation, redox properties, protein binding, and antiproliferative activity.
2007-05-03
Free radicals in vicarious C-amination reactions of 1-methyl-4-nitropyrazole.
2005-12
Scanning probe microscopy characterization of single chains based on a one-dimensional oxalato-bridged manganese(II) complex with 4-aminotriazole.
2005-11-14
[Sanitary standardization of 1-carbamoyl-3(5)-methylpyrazole, N-hydroxymethyl-3(5)-methylpyrazole and 4-amino-1,2,4-triazole in the water of reservoirs].
2002-01-29
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:06:34 GMT 2025
Edited
by admin
on Mon Mar 31 21:06:34 GMT 2025
Record UNII
O57Y04816H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-AMINO-1,2,4-TRIAZOLE
Systematic Name English
NSC-3263
Preferred Name English
4H-1,2,4-TRIAZOLE, 4-AMINO-
Systematic Name English
NSC-7242
Code English
Code System Code Type Description
ECHA (EC/EINECS)
209-533-5
Created by admin on Mon Mar 31 21:06:34 GMT 2025 , Edited by admin on Mon Mar 31 21:06:34 GMT 2025
PRIMARY
CAS
584-13-4
Created by admin on Mon Mar 31 21:06:34 GMT 2025 , Edited by admin on Mon Mar 31 21:06:34 GMT 2025
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EPA CompTox
DTXSID9033058
Created by admin on Mon Mar 31 21:06:34 GMT 2025 , Edited by admin on Mon Mar 31 21:06:34 GMT 2025
PRIMARY
NSC
7242
Created by admin on Mon Mar 31 21:06:34 GMT 2025 , Edited by admin on Mon Mar 31 21:06:34 GMT 2025
PRIMARY
FDA UNII
O57Y04816H
Created by admin on Mon Mar 31 21:06:34 GMT 2025 , Edited by admin on Mon Mar 31 21:06:34 GMT 2025
PRIMARY
PUBCHEM
11432
Created by admin on Mon Mar 31 21:06:34 GMT 2025 , Edited by admin on Mon Mar 31 21:06:34 GMT 2025
PRIMARY
NSC
3263
Created by admin on Mon Mar 31 21:06:34 GMT 2025 , Edited by admin on Mon Mar 31 21:06:34 GMT 2025
PRIMARY
MESH
C533754
Created by admin on Mon Mar 31 21:06:34 GMT 2025 , Edited by admin on Mon Mar 31 21:06:34 GMT 2025
PRIMARY