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

CAS: 36001-88-4 Cat. No.: A349467 Molecular Weight: 304.30 EC Number: 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

Overview

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

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]

Specifications & Purity

≥98%

Biochemical and Physiological Mechanisms

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.

Storage

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

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488187213
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488187213
• Canonical Smiles: 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)
• Isomeric SMILES: CC1=CC(=C(C=C1)OP(=S)(NC(C)C)OC)[N+](=O)[O-]
• Molecular Weight: 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
    • Class Benzene and substituted derivatives
      • Subclass Nitrobenzenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: 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
• Description: 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

Associated Targets(non-human)

Plasmodium falciparum (966862 Activities)

Explore this target

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

Mechanisms of Action

Chemical and Physical Properties

• Sensitivity: Light sensitive
• Melt Point(°C): 65° C
• Molecular Weight: 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