Carboxine - Moligand™, ≥98% , CAS No.5234-68-4

CAS: 5234-68-4 Cat. No.: C302005 Formule: C₁₂H₁₃NO₂S Poids moléculaire: 235.3 Numéro CE: 226-031-1

QUALITÉ & PURETÉ Moligand™, ≥98%

Synonyms

Karboxyn|Vitavax 100|Vitavax 735D|1, 5,6-dihydro-2-methyl-|Carboxin [ISO]|CARBOXIN [MI]|1, 2,3-dihydro-5-carboxanilido-6-methyl-|Vitavax-300|2,4-oxathiin-5-carboxanilide|1, 5,6-dihydro-2-methyl-N-phenyl-|5,6-Dihydro-2-methyl-1,4-oxathiin-3-carboxanilide|Cerevax|1,4-Oxathiin-3-carboxanilide, 5,6-dihydro-2-methyl-|Vitavax EC 200|2,3-Dihydro-6-methyl-5-phenylcarbamoyl-1,4-oxathiin|SDCCGMLS-0037038.P002|Vitavax 34|Vitavax 30-C|2,4-oxathiin|Cerevax Extra|1,4-Oxathiin-3-carboxamide, 5,6-dihydro-2-methyl-N-phenyl-|5,6-Dihydro-2-methyl-3-carboxanilido-1,4-oxathiin [German]|Enhance Plus|Vitaflo 250|CARBOXIN [HSDB]|Mist-O-Matic Murganic|2,3-Dihydro-5-carboxanilido-6-methyl-1,4-oxathiin|2-Methyl-N-phenyl-5,6-dihydro-1,4-oxathiine-3-carboxamide|Enhance|Pro-Gro|V 4X|Flo pro v seed protectant|RTV Vitavax|5-Carboxanilido-2,3-dihydro-6-methyl-1,4-oxathiin|Carboxine Form II|6-methyl-N-phenyl-2,3-dihydro-1,4-oxathiine-5-carboxamide|Kemikar|Cambridge id 5373048|Carboxine|DMOC|Vitavax-200|5,4-oxathiin-3-carboxanilide|DCMO|Carbathiin|Carbathiin;Vitavax;Kisvax;Carboxin|DMOC (VAN)|Germate Plus|Vitaflow|Carbathiine|Carboxine [ISO-French]|Kisvax|Vitavax 75W|5,6-Dihydro-2-methyl-3-carboxanilido-1,4-oxathiin|Carboxin [ANSI:BSI:ISO]|Dual Murganic RPB|Vitavax|1,4-Oxathiin, 2,3-dihydro-5-carboxanilido-6-methyl-|5,6-Dihydro-2-methyl-N-phenyl-1,4-oxathiin-3-carboxamide|CARBOXIN|Fenoxan|Vitavax-Thiram-Lindane

Storage

Room temperature,Desiccated

Shipped In

Normal

Vue d’ensemble

This product is a highly selective systemic fungicide that uses methods such as seed mixing, seed sealing, and seed soaking to prevent and control black ear disease in cereals such as barley, oats, corn, sorghum, and foxtail millet. It can also be used for foliar spraying to prevent rust diseases in wheat, beans, pears, cotton seedling diseases, as well as Verticillium wilt and Fusarium wilt. It can also be used as a wood preservative.

Spécifications

Synonymes

Karboxyn | Vitavax 100 | Vitavax 735D | 1, 5,6-dihydro-2-methyl- | Carboxin [ISO] | CARBOXIN [MI] | 1, 2,3-dihydro-5-carboxanilido-6-methyl- | Vitavax-300 | 2,4-oxathiin-5-carboxanilide | 1, 5,6-dihydro-2-methyl-N-phenyl- | 5,6-Dihydro-2-methyl-1,4-oxathiin-3-carboxanilide | Cerevax | 1,4-Oxathiin-3-carboxanilide, 5,6-dihydro-2-methyl- | Afficher plus

Spécifications et pureté

Moligand™, ≥98%

Conditions de stockage de stockage

Room temperature,Desiccated

Expédié en

Normal

Grade

Moligand™

Pureté

≥98%

Noms et identifiants

Pubchem Sid

528775524

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/528775524

Sourires canoniques

CC1=C(SCCO1)C(=O)NC2=CC=CC=C2

IUPAC Name

6-methyl-N-phenyl-2,3-dihydro-1,4-oxathiine-5-carboxamide

InChIKey

GYSSRZJIHXQEHQ-UHFFFAOYSA-N

INCHI

1S/C12H13NO2S/c1-9-11(16-8-7-15-9)12(14)13-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,13,14)

Isomères SMILES

CC1=C(SCCO1)C(=O)NC2=CC=CC=C2

Poids moléculaire

235.3

Reaxy-Rn

983249

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=983249&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: Anilides
• Alternative Parents: N-arylamides Oxathiins Vinylogous esters Thioenol ethers Secondary carboxylic acid amides Oxacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Anilide - N-arylamide - 1,4-oxathiin - Vinylogous ester - Carboxamide group - Secondary carboxylic acid amide - Thioenolether - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic nitrogen compound - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as anilides. These are organic heterocyclic compounds derived from oxoacids RkE(=O)l(OH)m (l not 0) by replacing an OH group by the NHPh group or derivative formed by ring substitution.
• External Descriptors: an amide

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 (humaines)

PTH1R Tclin Parathyroid hormone receptor (47172 Activities)

Discover Target: PTH1R

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AHR Tclin Aryl hydrocarbon receptor (1071 Activities)

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HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)

Discover Target: HSD17B10

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EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

Discover Target: EHMT2

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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

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GMNN Tbio Geminin (128009 Activities)

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microRNA 21 (64692 Activities)

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CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)

Discover Target: CBX1

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RAPGEF3 Tchem Rap guanine nucleotide exchange factor 3 (15528 Activities)

Discover Target: RAPGEF3

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Cibles associées (non humaines)

Ppard Peroxisome proliferator-activated receptor delta (358 Activities)

Discover Target: Ppard

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Mapk1 MAP kinase ERK2 (650 Activities)

Discover Target: Mapk1

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Oculimacula yallundae (312 Activities)

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Plasmodium falciparum (966862 Activities)

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Fusarium oxysporum (3998 Activities)

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Trypanosoma cruzi (99888 Activities)

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Puccinia recondita (281 Activities)

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L6 (7924 Activities)

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Luciferin 4-monooxygenase (66902 Activities)

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Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

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Nr1i2 Nuclear receptor subfamily 1 group I member 2 (14 Activities)

Discover Target: Nr1i2

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Fusarium graminearum (1554 Activities)

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Cytospora (178 Activities)

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Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Insoluble in water; Degree of Solubility in water: 147 mg/l 20 °C; Soluble in Acetone,Methanol
• Point d'éclair (°C): 100°C
• Point de fusion (°C): 93-95°C
• Poids moléculaire: 235.300 g/mol
• XLogP3: 2.100
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 235.067 Da
• Monoisotopic Mass: 235.067 Da
• Topological Polar Surface Area: 63.600 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 295.000
• 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