Cyantraniliprole - Moligand™, ≥99% , CAS No.736994-63-1

CAS: 736994-63-1 Cat. No.: C412252 Formule: C₁₉H₁₄BrClN₆O₂ Poids moléculaire: 473.71

GRADE & PURITY Moligand™, ≥99%

Synonyms

3-Bromo-1-(3-chloro-2-pyridinyl)-N-[4-cyano-2-methyl-6-[(methylamino)carbonyl]phenyl]-1H-pyrazole-5-carboxamide | DPX-HGW86 | HGW-86

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Vue d’ensemble

Information

Cyantraniliprole (HGW-86) is an insecticide of the ryanoid class. Cyantraniliprole(HGW-86) has activity against pests such as Diaphorina citri that have developed resistance to other insecticides.

Specifications

Synonymes

3-Bromo-1-(3-chloro-2-pyridinyl)-N-[4-cyano-2-methyl-6-[(methylamino)carbonyl]phenyl]-1H-pyrazole-5-carboxamide | DPX-HGW86 | HGW-86

Spécifications et pureté

Moligand™, ≥99%

Mécanismes biochimiques et physiologiques

Cyantraniliprole (HGW-86) is an insecticide of the ryanoid class. Cyantraniliprole(HGW-86) has activity against pests such as Diaphorina citri that have developed resistance to other insecticides.

Conditions de stockage de stockage

Store at -20°C

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

Moligand™

Pureté

≥99%

Noms et identifiants

• Pubchem Sid: 528773025
• Sourires canoniques: CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)NC)C#N
• IUPAC Name: 5-bromo-2-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]pyrazole-3-carboxamide
• InChIKey: DVBUIBGJRQBEDP-UHFFFAOYSA-N
• INCHI: 1S/C19H14BrClN6O2/c1-10-6-11(9-22)7-12(18(28)23-2)16(10)25-19(29)14-8-15(20)26-27(14)17-13(21)4-3-5-24-17/h3-8H,1-2H3,(H,23,28)(H,25,29)
• Isomères SMILES: CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)NC)C#N
• Poids moléculaire: 473.71
• Reaxy-Rn: 11325110
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11325110&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Anilides
• Intermediate Tree Nodes: Not available
• Direct Parent: Aromatic anilides
• Alternative Parents: Pyrazolylpyridines m-Toluamides Benzamides 2-heteroaryl carboxamides Benzonitriles Benzoyl derivatives Pyrazole-5-carboxamides Aryl chlorides Aryl bromides Heteroaromatic compounds Vinylogous amides Secondary carboxylic acid amides Nitriles Azacyclic compounds Organochlorides Organobromides Organic oxides Hydrocarbon derivatives Organooxygen compounds Organopnictogen compounds
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Aromatic anilide - 2-pyrazolylpyridine - Benzoic acid or derivatives - M-toluamide - Toluamide - Benzamide - 2-heteroaryl carboxamide - Benzoyl - Benzonitrile - Pyrazole-5-carboxamide - Toluene - Aryl halide - Aryl chloride - Pyridine - Aryl bromide - Azole - Vinylogous amide - Pyrazole - Heteroaromatic compound - Secondary carboxylic acid amide - Carboxamide group - Nitrile - Carbonitrile - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Organochloride - Organobromide - Organohalogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as aromatic anilides. These are aromatic compounds containing an anilide group in which the carboxamide group is substituted with an aromatic group. They have the general structure RNC(=O)R', where R= benzene, and R = aryl 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

Cibles associées (non humaines)

Spodoptera littoralis (798 Activities)

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Myzus persicae (1112 Activities)

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Plutella xylostella (1838 Activities)

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Bemisia tabaci (599 Activities)

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Ryanodien receptor (32 Activities)

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

Ryanodine receptor (15 Activities)

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

Mécanismes d'action

Propriétés chimiques et physiques

• Poids moléculaire: 473.700 g/mol
• XLogP3: 3.900
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 472.005 Da
• Monoisotopic Mass: 472.005 Da
• Topological Polar Surface Area: 113.000 Ų
• Heavy Atom Count: 29
• Formal Charge: 0
• Complexity: 672.000
• 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

Références

1. Wenqiu Song, Weihua Liu, Qianqian Wang, Lin Hao, Qiuhua Wu, Chun Wang.  (2025)  A recyclable and durable azo-linked porous organic polymer for fast enrichment and sensitive detection of diamide insecticides in environmental and food samples.  FOOD CHEMISTRY,      [PMID:40252448] [10.1016/j.foodchem.2025.144371]

2. Yang Bingnian, Peng Ziqin, Xia Guangping, Ruan Guihua, Huang Yipeng, Tang Ningli.  (2026)  Controllable synthesis of reticulated covalent organic polymers for the rapid extraction of triazine herbicides in vegetables prior to analysis by high-performance liquid chromatography.  MICROCHIMICA ACTA,  193  (3): (150).  [PMID:41663847] [10.1007/s00604-026-07841-x]