Phosmet - analytical standard, 100ug/ml in acetone , CAS No.732-11-6

CAS: 732-11-6 Cat. No.: I114895 Formula: C₁₁H₁₂NO₄PS₂ Peso molecolare: 317.32 Beilstein Registry Number: 264869 Numero EC: 211-987-4

QUALITÀ & PUREZZA Analytical standard, 100ug/ml in acetone

Synonyms

Fosmet|Imidan WP|N-(Dimethoxyphosphinothioylthiomethyl)phthalimide|Kemolate|O,O-Dimethyl phosphorodithioate S-ester with N-(mercaptomethyl)phthalimide|PMP (Pesticide)|Del-Phos (TN)|ORBISECT|R 1504|Stauffer R 1504|Opera_ID_1806|R-1504|USEPA/OPP Pesticide Code: 59201|N-(Mercaptomethyl)phthalimide S-(O,O-dimethyl phosphorodithioate)|Phthalimidomethyl O,O-dimethyl phosphorodithioate|Prolate I-E|S-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl] O,O-dimethyl phosphorodithioate|Del-Phos|Phosphorodithioic acid O,O-dimethyl ester S-ester with N-(mercaptomethyl) phthalimide|Phosphorodithioic acid, S-[(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl] O,O-dimethyl ester|S-((1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl) O,O-dimethy phosphorodithioate|Prolate 5 Dust|Safidon|PHOSMET [GREEN BOOK]|S-((1,3-Dioxo-2H-isoindol-2-yl)methyl) O,O-dimethyl phosphorodithioate|DECEMTION|PHOSMET (MART.)|PHOSMET [MART.]|S-[(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl] o,o-dimethyl dithiophosphate|Phosmet [BSI:ISO]|Phtalofos|Phosmet|O,O-Dimethyl S-(N-phthalimidomethyl)dithiophosphate|Ftalophos|PHOSMET [MI]|Phosmet [BAN:BSI:ISO]|Percolate|PHOSMET [ISO]|Phosmet-d6 100 Amicrog/mL in Acetone|Phosphorodithioic acid, S-((1,3-dihydro-1,3-dioxo-isoindol-2-yl)methyl) O,O-dimethyl ester|Phthalophos|Decemthion P-6|N-(MERCAPTOMETHYL) PHTHALIMIDE S-(O,O-DIMETHYL PHOSPHORODITHIOATE)|Phthalimido O,O-dimethyl phosphorodithioate|Phosmet (BAN)|Phosphorodithioic acid, O,O-dimethyl ester, S-ester with N-(mercaptomethyl)phthalimide|O,O-Dimethyl S-phthalimidomethyl phosphorothionate|Decemthion|O,O-Dimethyl S-(phthalimidomethyl)phosphorodithioate|S-((1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl) O,O-dimethyl phosphorodithioate|Poron (TN)|Imidathion|PORECT|Prolate E|S-((1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl) O,O-dimethyl phosphorodithioate|IMIDAN|N-(Mercaptomethyl)phthalimide S-(O,O-dimethyl phosphorothionate)|Simidan|Phosphorodithioic acid, S-((1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl) O,O-dimethyl ester|N-(Mercaptomethyl)phthalimide S-(O,O-dimethyl) phosphorodithioate|O,O-Dimethyl S-(phthalimidomethyl) dithiophosphate|O,O-Dimethyl S-phthalimidomethyl phosphorodithioate|ORDATOX|Smidan|Prolate 8-OS|(O,O-Dimethyl-phthalimidiomethyl-dithiophosphate)|2-(dimethoxyphosphinothioylsulfanylmethyl)isoindole-1,3-dione|DECEMTHIO|Phosmet [BAN]|Decemtion P-6|O,O-Dimethyl phthalimidomethyl phosphorodithioate|PHOSMET [HSDB]|DECEMTHION EK 20|O,O-Dimethyl S-(phthalimididomethyl)phosphorodithioate

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice,FedEx DG Service

Panoramica

Phosmet is a widely used, broad spectrum insecticide, which belongs to the phosphorodithioate subclass of organophosphates. It can find applications in having a control over insects in horticultural crops and ornamental plants. It can be used to control olive fruit fly (Bactrocera oleae, Dacus oleae), which can cause damage to the olive oil trees.

Specifiche

Sinonimi

Fosmet | Imidan WP | N-(Dimethoxyphosphinothioylthiomethyl)phthalimide | Kemolate | O,O-Dimethyl phosphorodithioate S-ester with N-(mercaptomethyl)phthalimide | PMP (Pesticide) | Del-Phos (TN) | ORBISECT | R 1504 | Stauffer R 1504 | Opera_ID_1806 | R-1504 | USEPA/OPP Pesticide Code: 59201 | N-(Mercaptomethyl)phthalimide S-(O,O-dimethyl ph Mostra altro

Specifiche e purezza

analytical standard, 100ug/ml in acetone

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Protected from light

Spedito in

Wet ice,FedEx DG Service

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

Standard analitico

Nomi e identificatori

Sorrisi canonici

COP(=S)(OC)SCN1C(=O)C2=CC=CC=C2C1=O

IUPAC Name

2-(dimethoxyphosphinothioylsulfanylmethyl)isoindole-1,3-dione

InChIKey

LMNZTLDVJIUSHT-UHFFFAOYSA-N

INCHI

1S/C11H12NO4PS2/c1-15-17(18,16-2)19-7-12-10(13)8-5-3-4-6-9(8)11(12)14/h3-6H,7H2,1-2H3

Isomeri SMILES

COP(=S)(OC)SCN1C(=O)C2=CC=CC=C2C1=O

WGK Germania

3

RTECS

TE2275000

Numero UN

3077

Gruppo di imballaggio

III

Peso molecolare

317.32

Beilstein

264869

Reaxy-Rn

264869

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=264869&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Isoindoles and derivatives
      • Subclass Isoindolines
        • Level5 Isoindolones
          • Level6 Phthalimides

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Isoindoles and derivatives
• Subclass: Isoindolines
• Intermediate Tree Nodes: Isoindolones
• Direct Parent: Phthalimides
• Alternative Parents: Isoindoles N-substituted carboxylic acid imides Dithiophosphate S-esters Dithiophosphate O-esters Benzenoids Sulfenyl compounds Organothiophosphorus compounds Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Phthalimide - Isoindole - Carboxylic acid imide, n-substituted - Dithiophosphate s-ester - Benzenoid - Dithiophosphate o-ester - Carboxylic acid imide - Organic dithiophosphate - Carboxylic acid derivative - Sulfenyl compound - Organothiophosphorus compound - Azacycle - Organic oxide - Organopnictogen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as phthalimides. These are aromatic heterocyclic compounds containing a 1,3-dioxoisoindoline moiety. They are imide derivatives of phthalic anhydrides.
• 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.

DOI: 10.1186/s13321-016-0174-y

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Meccanismi d'azione

Proprietà chimiche e fisiche

• Sensibilità: Light sensitive
• Punto di infiammabilità (°F): >100 °C
• Punto di infiammabilità (°C): >100°C
• Punto di fusione (°C): 71.9°C
• Peso molecolare: 317.300 g/mol
• XLogP3: 2.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 5
• Exact Mass: 316.995 Da
• Monoisotopic Mass: 316.995 Da
• Topological Polar Surface Area: 113.000 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 399.000
• 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