1.0 2010-04-08 22:09:29 UTC 2018-05-28 22:26:31 UTC FDB011147 Azimsulfuron Acetolactate synthase inhibitor. Post-emergence herbicide for control of Echinochloa subspecies, used especies on rice. 1-(4,6-Dimethoxy-2-pyrimidinyl)-3-[[1-methyl-4-(2-methyl-2H-tetrazol-5-yl)pyrazol-5-yl]sulfonyl]urea A 8947 Azimsulfuron Azimsulfuron [iso] Gulliver IN-A8947 N-[[(4,6-Dimethoxy-2-pyrimidinyl)amino]carbonyl]-1-methyl-4-(2-methyl-2H-tetrazol-5-yl)-1H-pyrazole-5-sulfonamide, 9CI C13H16N10O5S 424.395 424.102584362 1-(4,6-dimethoxypyrimidin-2-yl)-3-{[1-methyl-4-(2-methyl-2H-1,2,3,4-tetrazol-5-yl)-1H-pyrazol-5-yl]sulfonyl}urea azimsulfuron 120162-55-2 COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C2=C(C=NN2C)C2=NN(C)N=N2)=N1 InChI=1S/C13H16N10O5S/c1-22-11(7(6-14-22)10-18-21-23(2)19-10)29(25,26)20-13(24)17-12-15-8(27-3)5-9(16-12)28-4/h5-6H,1-4H3,(H2,15,16,17,20,24) MAHPNPYYQAIOJN-UHFFFAOYSA-N belongs to the class of organic compounds known as pyrimidinyl-2-sulfonylureas. These are aromatic heterocyclic compounds containing a pyrimidine ring which is substituted with a sulfonylurea at the ring 2-position. Pyrimidinyl-2-sulfonylureas Organic compounds Organic nitrogen compounds Organonitrogen compounds Sulfonylureas Aromatic heteromonocyclic compounds Alkyl aryl ethers Aminosulfonyl compounds Azacyclic compounds Carbonyl compounds Heteroaromatic compounds Hydrocarbon derivatives Organic carbonic acids and derivatives Organic oxides Organopnictogen compounds Organosulfonic acids and derivatives Pyrazoles Pyrimidines and pyrimidine derivatives Tetrazoles Alkyl aryl ether Aminosulfonyl compound Aromatic heteromonocyclic compound Azacycle Azole Carbonic acid derivative Carbonyl group Ether Heteroaromatic compound Hydrocarbon derivative Organic oxide Organic oxygen compound Organic sulfonic acid or derivatives Organoheterocyclic compound Organooxygen compound Organopnictogen compound Organosulfonic acid or derivatives Organosulfur compound Pyrazole Pyrimidine Pyrimidinyl-2-sulfonylurea Sulfonyl Tetrazole Sulfonylurea herbicides aromatic ether logp -0.26 ALOGPS logs -2.61 ALOGPS solubility 1.03e+00 g/l ALOGPS melting_point Mp 170° logp 0.71 ChemAxon pka_strongest_acidic 5.04 ChemAxon pka_strongest_basic 1.69 ChemAxon iupac 1-(4,6-dimethoxypyrimidin-2-yl)-3-{[1-methyl-4-(2-methyl-2H-1,2,3,4-tetrazol-5-yl)-1H-pyrazol-5-yl]sulfonyl}urea ChemAxon average_mass 424.395 ChemAxon mono_mass 424.102584362 ChemAxon smiles COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C2=C(C=NN2C)C2=NN(C)N=N2)=N1 ChemAxon formula C13H16N10O5S ChemAxon inchi InChI=1S/C13H16N10O5S/c1-22-11(7(6-14-22)10-18-21-23(2)19-10)29(25,26)20-13(24)17-12-15-8(27-3)5-9(16-12)28-4/h5-6H,1-4H3,(H2,15,16,17,20,24) ChemAxon inchikey MAHPNPYYQAIOJN-UHFFFAOYSA-N ChemAxon polar_surface_area 180.93 ChemAxon refractivity 133.81 ChemAxon polarizability 38.88 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 11 ChemAxon donor_count 2 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 20908 Specdb::CMs 130901 Specdb::CMs 138635 Specdb::MsMs 51582 Specdb::MsMs 51583 Specdb::MsMs 51584 Specdb::MsMs 129648 Specdb::MsMs 129649 Specdb::MsMs 129650 Specdb::MsMs 2407415 Specdb::MsMs 2407416 Specdb::MsMs 2407417 Specdb::MsMs 2531169 Specdb::MsMs 2531170 Specdb::MsMs 2531171 Specdb::NmrOneD 118338 Specdb::NmrOneD 118339 Specdb::NmrOneD 118340 Specdb::NmrOneD 118341 Specdb::NmrOneD 118342 Specdb::NmrOneD 118343 Specdb::NmrOneD 118344 Specdb::NmrOneD 118345 Specdb::NmrOneD 118346 Specdb::NmrOneD 118347 Specdb::NmrOneD 118348 Specdb::NmrOneD 118349 Specdb::NmrOneD 118350 Specdb::NmrOneD 118351 Specdb::NmrOneD 118352 Specdb::NmrOneD 118353 Specdb::NmrOneD 118354 Specdb::NmrOneD 118355 Specdb::NmrOneD 118356 Specdb::NmrOneD 118357 HMDB33145 #<Reference:0x000055ce32139308>