Dimethoate - analytical standard , CAS No.60-51-5

CAS: 60-51-5 Cat. No.: D109819 Summenformel: C₅H₁₂NO₃PS₂ Molekulargewicht: 229.25 Beilstein Registry Number: 1785339 EG-Nummer: 200-480-3

QUALITÄT & REINHEIT Analytical standard

Synonyms

Dimeton|Fostion MM|Lurgo|Racusan|8014 Bis HC|Fosfamid (USSR)|BI-58|Fosfamid|Sevigor|Tara|O,O-Dimethyl methylcarbamoylmethyl phosphorodithioate|Roxion|dimethoate|Phosphorodithioic acid, O,O-dimethyl ester, S-ester with 2-mercapto-N-methylacetamide|Rebelate|Systoate|Trimetion|O,O-dimethyl S-(2-(methylamino)-2-oxoethyl) dithiophosphate|Aadimethoal|N-Monomethylamide of O,O-dimethyldithiophosphorylacetic acid|Phosphorodithioic acid O,O-dimethyl ester, ester with 2-mercapto-N-methylacetamide|Rogor 40|Sistemin|Dimethoaat|Dimethoate [ANSI:BSI:ISO]|O,O-Dimethyl S-((methylcarbamoyl)methyl)phosphorodithioate|RCRA waste number P044|BI 58|Roxion UA|Cygon 4E|Experimental Insecticide 12,880|Salut|CL 12880|Fosfatox R|Phosphamide|Turbair|Phosphorodithioic acid, O,O-dimethyl S-(2-(methylamino)-2-oxoethyl)ester|American cyanamid 12880|Ditimur 40; ENT 24650; Experimental Insecticide 12880; FIP; Fosfatox R; Fosfotox|O,O-dimethyl S-[2-(methylamino)-2-oxoethyl]phosphorodithioate|Rogor L|Dimethogen|O,O-Dimethyl S-(N-methylcarbamoylmethyl) phosphorodithioate|O,O-Dimethyl S-methylcarbamoylmethyl phosphorodithioate|2-dimethoxyphosphinothioylsulfanyl-N-methylacetamide|Cygon 400|Dimevur|Fosfotox R 35|Solut|De-fend|Ferkethion|Fosfotox|Phosphamid|Rogor|O,O-Dimethyl S-(2-(methylamino)-2-oxoethyl)phosphorodithioate|O,O-Dimethyl S-(N-methylcarbamylmethyl) thiothionophosphate|O,O-Dimethyldithiophosphorylacetic acid, N-monomethylamide salt|S-Methylcarbamoylmethyl O,O-Dimethyl phosphorodithioate|Phosphorodithioic acid, O,O-dimethyl S-[2-(methylamino)-2-oxoethyl]ester|Tara 909|Cekuthoate|Cygon insecticide|O,O-dimethyl S-[2-(methylamino)-2-oxoethyl] phosphorodithioate|DIMETHOATE (MART.)|O,O-Dimethyl S-(2-(methylamino)-2-oxoethyl) phosphorodithioate|EI-12880|Fortion NM|Cygon|FIP|2-Dimethoxyphosphinothioylthio-N-methylacetamide|Daphene|Demos-L40|O,O-Dimethyl S-(N-methylcarbamoylmethyl) dithiophosphate|o,o-Dimethyl S-[2-(methylamino)-2-oxoethyl] dithiophosphate|Dimethoaat [Dutch]|Experimental Insecticide 12880|Dimetate|Dimethoat [German]|Dimethoate 30 EC|Fosfotox R|O,O-Dimethyl-S-(2-oxo-3-aza-butyl)-dithiophosphat [German]|Phosphorodithioic acid, O,O-dimethyl S-(2-(methylamino)-2-oxoethyl) ester|Dimethoat|Phosphorodithioic acid, O,O-dimethyl S-[2-(methylamino)-2-oxoethyl] ester|Cygon 2-E|DIMETHOATE [MART.]|PERFEKTHION S|Devigon|Perfecthion|Sinoratox

Storage

Store at 2-8°C

Shipped In

Wet ice

Spezifikationen

Synonyme

Dimeton | Fostion MM | Lurgo | Racusan | 8014 Bis HC | Fosfamid (USSR) | BI-58 | Fosfamid | Sevigor | Tara | O,O-Dimethyl methylcarbamoylmethyl phosphorodithioate | Roxion | dimethoate | Phosphorodithioic acid, O,O-dimethyl ester, S-ester with 2-mercapto-N-methylacetamide | Rebelate | Systoate | Trimetion | O,O-dimethyl S-(2-(methylamino) Show more

Spezifikationen & Reinheit

analytical standard

Biochemische und physiologische Mechanismen

类似于毒扁豆碱的乙酰胆碱酯酶的可逆抑制剂，但是不能穿过血脑屏障。

Storage

Store at 2-8°C

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Note

Analytischer Standard

Namen und Kennungen

Pubchem Sid

508811752

Kanonisches Lächeln

CNC(=O)CSP(=S)(OC)OC

IUPAC Name

2-dimethoxyphosphinothioylsulfanyl-N-methylacetamide

InChIKey

MCWXGJITAZMZEV-UHFFFAOYSA-N

INCHI

1S/C5H12NO3PS2/c1-6-5(7)4-12-10(11,8-2)9-3/h4H2,1-3H3,(H,6,7)

Isomere SMILES

CNC(=O)CSP(=S)(OC)OC

WGK Deutschland

3

UN-Nummer

2783(solid)3018(liquid)

Verpackungsgruppe

I

Molekulargewicht

229.25

Beilstein

1785339

Reaxy-Rn

1785339

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1785339&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Klasse Organic dithiophosphoric acids and derivatives
      • Subclass Dithiophosphate O-esters

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: Organic dithiophosphoric acids and derivatives
• Subclass: Dithiophosphate O-esters
• Intermediate Tree Nodes: Not available
• Direct Parent: Dithiophosphate O-esters
• Alternative Parents: Dithiophosphate S-esters Secondary carboxylic acid amides Sulfenyl compounds Organothiophosphorus compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Dithiophosphate s-ester - Dithiophosphate o-ester - Carboxamide group - Secondary carboxylic acid amide - Sulfenyl compound - Organothiophosphorus compound - Carboxylic acid derivative - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as dithiophosphate o-esters. These are o-ester derivatives of dithiophosphates, with the general structure RSP(O)(O)=S (R = organyl group).
• 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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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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VDR Tclin Vitamin D receptor (26531 Activities)

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RXRA Tclin Retinoid X receptor alpha (3637 Activities)

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ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

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NR1H4 Tclin Bile acid receptor FXR (6228 Activities)

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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

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GMNN Tbio Geminin (128009 Activities)

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PABPC1 Tbio Polyadenylate-binding protein 1 (2615 Activities)

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SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)

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SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)

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Aphis gossypii (526 Activities)

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Mapt Microtubule-associated protein tau (6 Activities)

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Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

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ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)

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Bactrocera oleae (43 Activities)

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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Empfindlichkeit: Light sensitive.
• Flammpunkt (°C): 2°C
• Siedepunkt (°C): 107°C
• Schmelzpunkt (°C): 52-52.5°C
• Molekulargewicht: 229.300 g/mol
• XLogP3: 0.800
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 5
• Exact Mass: 229 Da
• Monoisotopic Mass: 229 Da
• Topological Polar Surface Area: 105.000 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 191.000
• 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