Amiprofos methyl - ≥98% , CAS No.36001-88-4

CAS: 36001-88-4 Cat. No.: A349467 Formula: C₁₁H₁₇N₂O₄PS Peso molecolare: 304.30 Numero EC: 252-829-4

GRADE & PURITY ≥98%

Synonyms

BAY-NTN 6867 | O-Methyl 2-nitro-4-tolyl isopropylphosphoramidothioate | Tokunol M | NTN 2975 | N-[methoxy-(4-methyl-2-nitrophenoxy)phosphinothioyl]propan-2-amine | Amiprophos methyl | Amiprofos-methyl | Amiprofos-methyl [ISO]

Storage

Store at 2-8°C,Protected from light,Argon charged

Shipped In

Wet ice

Panoramica

Amiprofos methyl is a herbicide that prevents microtubule polymerization in plant cells, but not animal cells. Crop plants resistant to amiprofos-methyl and several other herbicides have been developed.

Specifications

Sinonimi

BAY-NTN 6867 | O-Methyl 2-nitro-4-tolyl isopropylphosphoramidothioate | Tokunol M | NTN 2975 | N-[methoxy-(4-methyl-2-nitrophenoxy)phosphinothioyl]propan-2-amine | Amiprophos methyl | Amiprofos-methyl | Amiprofos-methyl [ISO]

Specifiche e purezza

≥98%

Meccanismi biochimici e fisiologici

Herbicide that prevents microtubule polymerization in plant cells, but not animal cells. Crop plants resistant to amiprofos-methyl and several other herbicides have been developed by insertion of a xenobiotic-detoxifying human gene CYP2B6.

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Protected from light,Argon charged

Spedito in

Wet ice

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

Purezza

≥98%

Nomi e identificatori

• Pubchem Sid: 488187213
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488187213
• Sorrisi canonici: CC1=CC(=C(C=C1)OP(=S)(NC(C)C)OC)[N+](=O)[O-]
• IUPAC Name: N-[methoxy-(4-methyl-2-nitrophenoxy)phosphinothioyl]propan-2-amine
• InChIKey: VHEWQRWLIDWRMR-UHFFFAOYSA-N
• INCHI: 1S/C11H17N2O4PS/c1-8(2)12-18(19,16-4)17-11-6-5-9(3)7-10(11)13(14)15/h5-8H,1-4H3,(H,12,19)
• Isomeri SMILES: CC1=CC(=C(C=C1)OP(=S)(NC(C)C)OC)[N+](=O)[O-]
• Peso molecolare: 304.30
• Reaxy-Rn: 2000833
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2000833&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Nitrobenzenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Nitrobenzenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Nitrobenzenes
• Alternative Parents: Nitrotoluenes Phenoxy compounds Nitroaromatic compounds Thiophosphoric acid esters Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Nitrobenzene - Nitrotoluene - Phenoxy compound - Nitroaromatic compound - Toluene - Thiophosphoric acid ester - Organic thiophosphoric acid or derivatives - C-nitro compound - Organic nitro compound - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as nitrobenzenes. These are compounds containing a nitrobenzene moiety, which consists of a benzene ring with a carbon bearing a nitro group.
• External Descriptors: Not available

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

Obiettivi associati (non umani)

Plasmodium falciparum (966862 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Sensibilità: Light sensitive
• Punto di fusione (°C): 65° C
• Peso molecolare: 304.300 g/mol
• XLogP3: 3.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 5
• Exact Mass: 304.065 Da
• Monoisotopic Mass: 304.065 Da
• Topological Polar Surface Area: 108.000 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 361.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1