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flumioxazin - analytical standard, high purity , CAS No.103361-09-7

4 Citations COA COA
In stock
Item Number
F114497
Grouped product items
SKU Size
Availability
 Price Qty
F114497-100mg
100mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$687.90
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Bulk Order  SDS  DATASHEET  Specification Sheet

Basic Description

Synonyms Flumioxazin | 103361-09-7 | Sumisoya | Flumioxazin [ISO] | S-53482 | S 53482 | V 53482 | CHEBI:8939 | EINECS Annex I Index 613-166-00-X | Sumisoya; V 53482 | L0PX7OGI22 | Flumioxazine | DTXSID7032555 | 7-Fluoro-6-(3,4,5,6-tetrahydrophthalimido)-4-(2-propynyl)-1,4-benzoxazin-3(2H)-
Specifications & Purity analytical standard
Shipped In Normal
Grade analytical standard

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Benzoxazines
Subclass Benzoxazinones
Intermediate Tree Nodes Not available
Direct Parent Benzoxazinones
Alternative Parents Benzomorpholines  Isoindolones  Isoindoles  Alkyl aryl ethers  Maleimides  Aryl fluorides  Benzenoids  N-substituted carboxylic acid imides  Dicarboximides  Pyrrolines  Tertiary carboxylic acid amides  Lactams  Oxacyclic compounds  Acetylides  Azacyclic compounds  Organonitrogen compounds  Organopnictogen compounds  Hydrocarbon derivatives  Carbonyl compounds  Organic oxides  Organofluorides  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Benzoxazinone - Isoindolone - Benzomorpholine - Isoindole or derivatives - Isoindole - Maleimide - Alkyl aryl ether - Benzenoid - Oxazinane - Carboxylic acid imide, n-substituted - Aryl fluoride - Aryl halide - Carboxylic acid imide - Dicarboximide - Tertiary carboxylic acid amide - Pyrroline - Carboxamide group - Lactam - Acetylide - Carboxylic acid derivative - Oxacycle - Azacycle - Ether - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as benzoxazinones. These are organic compounds containing a benzene fused to an oxazine ring (a six-member aliphatic ring with four carbon atoms, one oxygen atom, and one nitrogen atom) bearing a ketone group.
External Descriptors benzoxazine

Associated Targets(non-human)

Echinochloa crus-galli (3685 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Amaranthus (163 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Arachis hypogaea (20 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Oryza sativa (2923 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Zea mays (820 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Glycine max (342 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Setaria viridis (435 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Triticum aestivum (1582 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Abutilon theophrasti (831 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Amaranthus retroflexus (1838 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Chenopodium album (769 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Digitaria sanguinalis (1594 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Gossypium hirsutum (233 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Phaseolus vulgaris (518 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Protoporphyrinogen IX oxidase (35 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PPXI Protoporphyrinogen oxidase, chloroplastic (33 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Brassica rapa subsp. oleifera (1696 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Gossypium (36 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Amaranthus blitum (48 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Erigeron canadensis (118 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Scenedesmus acutus (534 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name 2-(7-fluoro-3-oxo-4-prop-2-ynyl-1,4-benzoxazin-6-yl)-4,5,6,7-tetrahydroisoindole-1,3-dione
INCHI InChI=1S/C19H15FN2O4/c1-2-7-21-15-9-14(13(20)8-16(15)26-10-17(21)23)22-18(24)11-5-3-4-6-12(11)19(22)25/h1,8-9H,3-7,10H2
InChIKey FOUWCSDKDDHKQP-UHFFFAOYSA-N
Smiles C#CCN1C(=O)COC2=CC(=C(C=C21)N3C(=O)C4=C(C3=O)CCCC4)F
Isomeric SMILES C#CCN1C(=O)COC2=CC(=C(C=C21)N3C(=O)C4=C(C3=O)CCCC4)F
WGK Germany 3
Molecular Weight 354.33
Reaxy-Rn 8290535
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8290535&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot Number Certificate Type Date Item
H2430468 Certificate of Analysis Jun 27, 2024 F114497
E1923061 Certificate of Analysis Jan 05, 2023 F114497

Chemical and Physical Properties

Melt Point(°C) 201-204°C
Molecular Weight 354.300 g/mol
XLogP3 1.800
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 5
Rotatable Bond Count 2
Exact Mass 354.102 Da
Monoisotopic Mass 354.102 Da
Topological Polar Surface Area 66.900 Ų
Heavy Atom Count 26
Formal Charge 0
Complexity 724.000
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

Citations of This Product

How to Cite Aladdin Scientific Products?
1. Yu-Han Sun, Liu Yang, Xian-Xian Ji, Yuan-Zhen Wang, Yu-Long Liu, Ying Fu, Fei Ye.  (2024)  Efficient detection of flusilazole by an electrochemical sensor derived from MOF MIL-53(Fe) for food safety.  FOOD CHEMISTRY,  440  (138244). 
2. Ling Jia, Li-Xia Zhao, Fang Sun, Jie Peng, Jia-Yu Wang, Xin-Yu Leng, Shuang Gao, Ying Fu, Fei Ye.  (2022)  Diazabicyclo derivatives as safeners protect cotton from injury caused by flumioxazin.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,  187  (105185). 
3. Wei-Chuang Kong, Chen-Chen Li, Ai-Hong Zhang, Xin-Long Li, Qian-Rui Gong, Bing-Tan Jin, Xiao-Juan Jia, Xu-Ying Liu, Yan-Fei Kang.  (2024)  A colorimetric-aptamer-based assay for the determination of enrofloxacin through triggering the aggregation of gold nanoparticles.  Analytical Methods,     
4. Yuan-Zhen Wang, Liu Yang, Jia-Jia Kou, Yu-Qing Zhan, Yi-Lin Niu, Yu-Long Liu.  (2025)  High-temperature calcined Mn-MOF derivative for electrochemical detection of flumioxazin in environmental and food samples.  POLYHEDRON,  275  (117525). 

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