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Azamethiphos - 10mM in DMSO, high purity , CAS No.35575-96-3
Basic Description
Synonyms
Azamethiphos | 35575-96-3 | Ciba-Geigy 18809 | OMS No 1825 | CGA 18809 | Azamethiphos [BAN] | Azamethiophos | S-((6-Chloro-2-oxooxazolo[4,5-b]pyridin-3(2H)-yl)methyl) O,O-dimethyl phosphorothioate | S-6-Chloro-2,3-dihydro-2-oxo-1,3-oxazolo(4,5-b)pyridin-3-ylmethyl O,O-di
Specifications & Purity
10mM in DMSO
Storage Temp
Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Oxazolopyridines
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Oxazolopyridines
Alternative Parents
Pyridines and derivatives Aryl chlorides Oxazoles Heteroaromatic compounds Sulfenyl compounds Oxacyclic compounds Organothiophosphorus compounds Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organochlorides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1,3-oxazolopyridine - Aryl chloride - Aryl halide - Pyridine - Azole - Oxazole - Heteroaromatic compound - Azacycle - Sulfenyl compound - Organothiophosphorus compound - Oxacycle - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organic oxygen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as oxazolopyridines. These are polycyclic compounds containing an oxazole ring fused to a pyridine ring.
External Descriptors
Organophosphorus insecticides
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
6-chloro-3-(dimethoxyphosphorylsulfanylmethyl)-[1,3]oxazolo[4,5-b]pyridin-2-one
INCHI
InChI=1S/C9H10ClN2O5PS/c1-15-18(14,16-2)19-5-12-8-7(17-9(12)13)3-6(10)4-11-8/h3-4H,5H2,1-2H3
InChIKey
VNKBTWQZTQIWDV-UHFFFAOYSA-N
Smiles
COP(=O)(OC)SCN1C2=C(C=C(C=N2)Cl)OC1=O
Isomeric SMILES
COP(=O)(OC)SCN1C2=C(C=C(C=N2)Cl)OC1=O
UN Number
2811
Packing Group
III
Molecular Weight
324.68
Reaxy-Rn
1086470
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1086470&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Molecular Weight
324.680 g/mol
XLogP3
1.000
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
7
Rotatable Bond Count
5
Exact Mass
323.974 Da
Monoisotopic Mass
323.974 Da
Topological Polar Surface Area
103.000 Ų
Heavy Atom Count
19
Formal Charge
0
Complexity
393.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
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