Home Carboxys 2-Thiophenecarboxylic acid hydrazide

2-Thiophenecarboxylic acid hydrazide

CAS No.:
2361-27-5
Catalog Number:
AG003HY9
Molecular Formula:
C5H6N2OS
Molecular Weight:
142.1789
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$15
- +
25g
98%
In Stock USA
United States
$62
- +
100g
98%
In Stock USA
United States
$238
- +
Product Description
Catalog Number:
AG003HY9
Chemical Name:
2-Thiophenecarboxylic acid hydrazide
CAS Number:
2361-27-5
Molecular Formula:
C5H6N2OS
Molecular Weight:
142.1789
MDL Number:
MFCD00005435
IUPAC Name:
thiophene-2-carbohydrazide
InChI:
InChI=1S/C5H6N2OS/c6-7-5(8)4-2-1-3-9-4/h1-3H,6H2,(H,7,8)
InChI Key:
SOGBOGBTIKMGFS-UHFFFAOYSA-N
SMILES:
NNC(=O)c1cccs1
EC Number:
219-107-0
Properties
Complexity:
118  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
142.02g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
142.176g/mol
Monoisotopic Mass:
142.02g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
83.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.6  
Literature
Title Journal
(1Z,2E)-N'-{1-[2-(4-Bromo-phen-yl)hydrazin-1-yl-idene]-1-chloro-propan-2-yl-idene}thio-phene-2-carbohydrazide. Acta crystallographica. Section E, Structure reports online 20120501
2-(5-Bromo-pyridin-3-yl)-5-[3-(4,5,6,7-tetra-hydro-thieno[3,2-c]pyridine-5-ylsulfon-yl)thio-phen-2-yl]-1,3,4-oxa-diazole. Acta crystallographica. Section E, Structure reports online 20111001
2-(Biphenyl-4-yl)-5-[3-(4,5,6,7-tetra-hydro-thieno[3,2-c]pyridine-5-ylsulfon-yl)thio-phen-2-yl]-1,3,4-oxa-diazole. Acta crystallographica. Section E, Structure reports online 20111001
N'-[1-(2-Hy-droxy-phen-yl)ethyl-idene]thio-phene-2-carbohydrazide. Acta crystallographica. Section E, Structure reports online 20110101
N'-Benzyl-idene-thio-phene-2-carbohydrazide. Acta crystallographica. Section E, Structure reports online 20110101
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. Bioorganic & medicinal chemistry letters 20101101
Design and synthesis of novel thiophenecarbohydrazide, thienopyrazole and thienopyrimidine derivatives as antioxidant and antitumor agents. Acta pharmaceutica (Zagreb, Croatia) 20100901
N'-(4-Hy-droxy-benzyl-idene)thio-phene-2-carbohydrazide. Acta crystallographica. Section E, Structure reports online 20100701
Nucleophilic catalysis of acylhydrazone equilibration for protein-directed dynamic covalent chemistry. Nature chemistry 20100601
N'-(4-Methyl-benzyl-idene)thio-phene-2-carbohydrazide. Acta crystallographica. Section E, Structure reports online 20100601
(E)-N'-(4-Methoxy-benzyl-idene)thio-phene-2-carbohydrazide. Acta crystallographica. Section E, Structure reports online 20100601
N'-(4-Cyano-benzyl-idene)thio-phene-2-carbohydrazide. Acta crystallographica. Section E, Structure reports online 20100601
N'-(4-Bromo-benzyl-idene)thio-phene-2-carbohydrazide. Acta crystallographica. Section E, Structure reports online 20100401
N'-(4-Chloro-benzyl-idene)thio-phene-2-carbohydrazide. Acta crystallographica. Section E, Structure reports online 20100401
N'-[(5-Methyl-2-fur-yl)methyl-ene]thio-phene-2-carbohydrazide. Acta crystallographica. Section E, Structure reports online 20100401
Lipophilic aroylhydrazone chelator HNTMB and its multiple effects on ovarian cancer cells. BMC cancer 20100101
Multinuclear magnetic resonance, electrospray ionization-mass spectroscopy, and parametric method 5 studies of a new derivative of gossypol with 2-thiophenecarbohydrazide as well as its complexes with LI+, Na+, K+, RB+, and Cs+ cations. Biopolymers 20061015
Prediction of genotoxicity of chemical compounds by statistical learning methods. Chemical research in toxicology 20050601
Crystal structures of the RNA-dependent RNA polymerase genotype 2a of hepatitis C virus reveal two conformations and suggest mechanisms of inhibition by non-nucleoside inhibitors. The Journal of biological chemistry 20050506
Reduction of tetrazolium salts containing heterocyclic compounds by tubercle bacilli. The American review of respiratory disease 19730101
Properties