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· · COA & SDS available for every product · Same-day shipping on in-stock items Diflubenzuron - ≥97% , CAS No.35367-38-5
Synonyms
Benzamide, N-[[(4-chlorophenyl)amino]carbonyl]-2,6-difluoro-|N-{[(4-chlorophenyl)amino]carbonyl}-2,6-difluorobenzamide|Cambridge id 5259978|Diflubenzuron;N-[[(4-Chlorophenyl)amino]carbonyl]-2,6-di-fluorobenzamide;1-(4-Chlorophenyl)-3-(2,6-difluorobenzoyl)urea;Difluron;Dimilin|DIFLUBENZURON [MART.]|PDD 6040I|1-(4-Chlorophenyl)-3-(2,6-difluorobenzoyl)urea|Diflubenzuron [ANSI:BSI:ISO]|Benzamide, N-(((4-chlorophenyl)amino)carbonyl)-2,6-difluoro-|1-(p-Chlorophenyl)-3-(2,6-difluorobenzoyl)urea|1-(p-Chlorophenyl)-3-(2,6-difluorobenzoyl)-Urea|N-[(4-chloroanilino)-oxomethyl]-2,6-difluorobenzamide|N-(4-Chlorophenyl)-N'-(2,6-difluorobenzoyl)urea|Dimilin ODC-45|Thompson-hayward TH6040|Urea, 1-(p-chlorophenyl)-3-(2,6-difluorobenzoyl)-|3-(4-chlorophenyl)-1-[(2,6-difluorophenyl)carbonyl]urea|Philips-duphar PH 60-40|Difubenzuron|DIFLUBENZURON|Astonex|Difluron|N-(4-Chlorophenyl)-N'-(2,6-difluorobenzoyl)urea #|N-[[(4-Chlorophenyl)amino]carbonyl]-2,6-difluorobenzamide, 9CI|Larvakil|Dimilin WP-25|N-(4-Chlorophenylcarbamoyl)-2,6-difluorobenzamide|Duphacid|N-((4-Chlorophenyl)carbamoyl)-2,6-difluorobenzamide|TH 6040|1-(4-Chlorophenyl)-3-(2,6-difluorobenzoyl)urea (diflubenzuron)|N-[(4-chlorophenyl)carbamoyl]-2,6-difluorobenzamide|IFLUBENZURON|N-[[(4-Chlorophenyl)amno]carbonyl]-2,6-difluorobenzamide|Thompson-Hayward 6040|DIFLUBENZURON [HSDB]|DIFLUBENZURON [JAN]|DIFLUBENZURON [MI]|Thompson Hayward 6040|1-(4-chlorophenyl)-3-[(2,6-difluorophenyl)carbonyl]urea|Dimilin|Dioflubenzuron|N-(((4-Chlorophenyl)amino)carbonyl)-2,6-difluorobenzamide|1-(4-Chlorophenyl)-3-(2,6-difluorobenzyl)urea|n-[[(4-chlorophenyl)amino]carbonyl]-2,6-difluorobenzamide|Dimilin G4
Overview Diflubenzuron is a benzoyl-urea insecticide, found to be a potent inhibitor of melanosome synthesis in mouse melanoma cells. Diflubenzuron has also been shown to inhibit TCDD-induced CYP1A1 expression in HepG2 cells.
Specifications Synonyms
Benzamide, N-[[(4-chlorophenyl)amino]carbonyl]-2,6-difluoro- | N-{[(4-chlorophenyl)amino]carbonyl}-2,6-difluorobenzamide | Cambridge id 5259978 | Diflubenzuron;N-[[(4-Chlorophenyl)amino]carbonyl]-2,6-di-fluorobenzamide;1-(4-Chlorophenyl)-3-(2,6-difluorobenzoyl)urea;Difluron;Dimilin | DIFLUBENZURON [MART.] | PDD 6040I | 1-(4-Chlorophenyl)- Show more
Specifications & Purity
≥97%
Names and Identifiers Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504753557
Canonical Smiles
C1=CC(=C(C(=C1)F)C(=O)NC(=O)NC2=CC=C(C=C2)Cl)F
IUPAC Name
N-[(4-chlorophenyl)carbamoyl]-2,6-difluorobenzamide
InChIKey
QQQYTWIFVNKMRW-UHFFFAOYSA-N
INCHI
1S/C14H9ClF2N2O2/c15-8-4-6-9(7-5-8)18-14(21)19-13(20)12-10(16)2-1-3-11(12)17/h1-7H,(H2,18,19,20,21)
Isomeric SMILES
C1=CC(=C(C(=C1)F)C(=O)NC(=O)NC2=CC=C(C=C2)Cl)F
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2162461&ln=
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Benzenoids Class Benzene and substituted derivatives Subclass N-phenylureas Intermediate Tree Nodes N-acyl-phenylureas Direct Parent N-benzoyl-N'-phenylureas Alternative Parents 2-halobenzoic acids and derivatives Benzoyl derivatives Chlorobenzenes Fluorobenzenes Aryl chlorides Aryl fluorides Vinylogous halides Ureas Carboxylic acids and derivatives Hydrocarbon derivatives Organic oxides Carbonyl compounds Organochlorides Organofluorides Organonitrogen compounds Organopnictogen compounds Molecular Framework Aromatic homomonocyclic compounds Substituents N-benzoyl-n'-phenylurea - Halobenzoic acid or derivatives - 2-halobenzoic acid or derivatives - Benzoic acid or derivatives - Benzoyl - Chlorobenzene - Fluorobenzene - Halobenzene - Aryl chloride - Aryl fluoride - Aryl halide - Vinylogous halide - Urea - Carbonic acid derivative - Carboxylic acid derivative - Organic nitrogen compound - Organohalogen compound - Organochloride - Organofluoride - Organonitrogen compound - Organooxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as n-benzoyl-n'-phenylureas. These are n-acyl-phenylureas that have the acyl group substituted by a phenyl group. External Descriptors Pesticides 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.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates (CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Soluble in methanol, DMSO, acetone (6.5 mg/ml at 20 °C), and ethanol. Insoluble in water. x_melt_point_char 230-232°C Molecular Weight 310.680 g/mol XLogP3 3.900 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 2 Exact Mass 310.032 Da Monoisotopic Mass 310.032 Da Topological Polar Surface Area 58.200 Ų Heavy Atom Count 21 Formal Charge 0 Complexity 379.000 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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