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Home Amines 20939-15-5
20939-15-5,MFCD00100277
Catalog No.:AA00I3XD

20939-15-5 | 4-Amino-5-methyl-4H-1,2,4-triazole-3-thiol

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100mg
95%
in stock  
$150.00   $105.00
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1g
95%
in stock  
$531.00   $372.00
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5g
95%
in stock  
$1,504.00   $1,053.00
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  • Technical Information
  • Properties
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Technical Information
Catalog Number:
AA00I3XD
Chemical Name:
4-Amino-5-methyl-4H-1,2,4-triazole-3-thiol
CAS Number:
20939-15-5
Molecular Formula:
C3H6N4S
Molecular Weight:
130.1715
MDL Number:
MFCD00100277
SMILES:
Cc1nnc(n1N)S
NSC Number:
527797
Properties
Computed Properties
 
Complexity:
151  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
XLogP3:
-0.8  

Literature

Title: New 1,2,4-triazole-based azo-azomethine dyes. Part II: synthesis, characterization, electrochemical properties and computational studies.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20121101

Title: Synthesis, characterization, and antibacterial studies of mixed ligand dioxouranium complexes with 8-hydroxyquinoline and some amino acids.

Journal: ISRN pharmaceutics 20110101

Title: 3-Methyl-4-[(E)-3-thien-ylmethyl-idene-amino]-1H-1,2,4-triazole-5(4H)-thione.

Journal: Acta crystallographica. Section E, Structure reports online 20101101

Title: (E)-3-Methyl-4-[(2-oxidoquinolin-1-ium-3-yl)methyl-eneamino]-1H-1,2,4-triazole-5(4H)-thione N,N-dimethyl-formamide solvate.

Journal: Acta crystallographica. Section E, Structure reports online 20091201

Title: 4-(4-Oxopent-2-en-2-yl-amino)-1,2,4-triazol-1-ium-5-thiol-ate.

Journal: Acta crystallographica. Section E, Structure reports online 20090701

Title: [Synthesis and antibacterial activity of 3-(4-amino-5-methyl-s-triazol-3-sulfanyl)-1-phenyl-propan-1-one O-(5-substituted phenyl-[1,3,4] oxadiazol-2-methyl)-oximes].

Journal: Yao xue xue bao = Acta pharmaceutica Sinica 20061201

Title: Synthesis, characterization and biological studies of Co(II), Ni(II), Cu(II) and Zn(II) complexes with bidentate Schiff bases derived by heterocyclic ketone.

Journal: European journal of medicinal chemistry 20060101

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