chempirical

Clothianidin

C6H8ClN5O2SCAS 210880-92-5249.67 g/mol

Open in Covalent MOL file
NNHNClSNHN+OO−
Aryl halideGuanidineNitro

Properties

Molecular formula
C6H8ClN5O2S
Molar mass
249.67 g/mol
Exact mass
249.0087 Da
Melting point
172–174 °C
logP
0.65Crippen estimate
Polar surface area
92.5 Ų
H-bond donors / acceptors
2 / 5
Rotatable bonds
3

Identifiers

CAS number
210880-92-5
SMILES
CN=C(NCc1cnc(Cl)s1)N[N+](=O)[O-]
InChIKey
PGOOBECODWQEAB-UHFFFAOYSA-N
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)

Weigh it out

Type any one amount. The others follow from the molar mass.

Names and synonyms

30 names · show all
  • Guanidine, N-[(2-chloro-5-thiazolyl)methyl]-N′-methyl-N′′-nitro-, [C(E)]-
  • [C(E)]-N-[(2-Chloro-5-thiazolyl)methyl]-N′-methyl-N′′-nitroguanidine
  • TI 435
  • Poncho
  • Dantotsu
  • Fullswing
  • Apacz
  • Clutch
  • Clutch (insecticide)
  • Belay
  • TM 44401
  • Arena
  • V 10170
  • Takeloc MC 50E
  • Takeloc CLMN 10
  • Celero
  • (E)-1-(2-Chloro-1,3-thiazol-5-yl methyl)-3-methyl-2-nitroguanidine
  • Poncho 600
  • Dantop
  • (E)-1-(2-Chloro-1,3-thiazole-5-ylmethyl)-3-methyl-2-nitroguanidine
  • Poncho 250
  • NipsIt Inside
  • Titan ST
  • Dantotsu 16WSG
  • Takeloc MC 50 super
  • NipsIt
  • (E)-1-(2-Chloro-1,3-thiazol-5-ylmethyl)-3-methyl-2-nitroguanidine
  • Nipsit inside insecticide
  • Takelock MC 50 super
  • Poncho 60 FS

Work with Clothianidin

Predict the NMR spectrum1H and 13C shifts with multiplicities Make a solutionWhat to weigh for any molarity and volume Check drug-likenessLipinski, Veber and lead-likeness Isotope patternExact mass and the mass spectrum pattern

Similar compounds

Dinotefuran165252-70-040 % similar Thiamethoxam153719-23-438 % similar 2-Chloro-5-(chloromethyl)thiazole105827-91-636 % similar 1-[(6-Chloro-3-pyridinyl)methyl]-4,5-dihydro-N-nitro-1H-imidazol-2-amine105827-78-936 % similar Imidacloprid138261-41-336 % similar 4,5-Dihydro-N-nitro-1H-imidazol-2-amine5465-96-334 % similar

Tanimoto similarity of circular fingerprints over the whole catalogue. All similar compounds

Elsewhere

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