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Home Halogens Guanidine, N-[(2-chloro-5-thiazolyl)methyl]-N'-methyl-N''-nitro-, [C(E)]-

Guanidine, N-[(2-chloro-5-thiazolyl)methyl]-N'-methyl-N''-nitro-, [C(E)]-

CAS No.:
210880-92-5
Catalog Number:
AG00I415
Molecular Formula:
Molecular Weight:
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Product Description
Catalog Number:
AG00I415
Chemical Name:
Guanidine, N-[(2-chloro-5-thiazolyl)methyl]-N'-methyl-N''-nitro-, [C(E)]-
CAS Number:
210880-92-5
MDL Number:
MFCD06200753
IUPAC Name:
1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3-methyl-2-nitroguanidine
InChI:
InChI=1S/C6H8ClN5O2S/c1-8-6(11-12(13)14)10-3-4-2-9-5(7)15-4/h2H,3H2,1H3,(H2,8,10,11)
InChI Key:
PGOOBECODWQEAB-UHFFFAOYSA-N
UNII:
2V9906ABKQ
Properties
Complexity:
258  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1  
Exact Mass:
249.009g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
249.673g/mol
Monoisotopic Mass:
249.009g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
123A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.3  
Literature
Title Journal
The neonicotinoid insecticide Clothianidin adversely affects immune signaling in a human cell line. Scientific reports 20170101
The combined effect of clothianidin and environmental stress on the behavioral and reproductive function in male mice. The Journal of veterinary medical science 20151001
Identification of key amino acid differences contributing to neonicotinoid sensitivity between two nAChR α subunits from Pardosa pseudoannulata. Neuroscience letters 20150101
Determination of the effects on learning and memory performance and related gene expressions of clothianidin in rat models. Cognitive neurodynamics 20141001
Activation and modulation of human α4β2 nicotinic acetylcholine receptors by the neonicotinoids clothianidin and imidacloprid. Journal of neuroscience research 20110801
A nicotinic acetylcholine receptor mutation (Y151S) causes reduced agonist potency to a range of neonicotinoid insecticides. Journal of neurochemistry 20061101
Neo-nicotinoid metabolic activation and inactivation established with coupled nicotinic receptor-CYP3A4 and -aldehyde oxidase systems. Toxicology letters 20060220
Properties