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Thiophanate-methyl

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Kiljanek, Tomasz; Niewiadowska, Alicja; Semeniuk, Stanisław; Gaweł, Marta; Borzęcka, Milena; Posyniak, Andrzej (2016). "Multi-residue method for the determination of pesticides and pesticide metabolites in honeybees by liquid and gas chromatography coupled with tandem mass spectrometry—Honeybee
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Romero-González, R.; Garrido Frenich, A.; Martínez Vidal, J.L.; Prestes, O.D.; Grio, S.L. (2011). "Simultaneous determination of pesticides, biopesticides and mycotoxins in organic products applying a quick, easy, cheap, effective, rugged and safe extraction procedure and ultra-high performance
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Mol, Hans G. J.; Plaza-Bolaños, Patricia; Zomer, Paul; De Rijk, Theo C.; Stolker, Alida A. M.; Mulder, Patrick P. J. (2008). "Toward a Generic Extraction Method for Simultaneous Determination of Pesticides, Mycotoxins, Plant Toxins, and Veterinary Drugs in Feed and Food Matrixes".
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Methods for its analysis have received considerable attention. It is commonly used to treat botrytis bunch rot and gray mold caused by
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InChI=1S/C12H14N4O4S2/c1-19-11(17)15-9(21)13-7-5-3-4-6-8(7)14-10(22)16-12(18)20-2/h3-6H,1-2H3,(H2,13,15,17,21)(H2,14,16,18,22)
434: 414:. The compound is a colorless or white solid, although commercial samples are generally tan-colored. It is prepared from 379: 183: 204: 596: 669: 146: 750: 588:"Grey mould of strawberry, a devastating disease caused by the ubiquitous necrotrophic fungal pathogen 659:
Cosseboom, Scott D.; Ivors, Kelly L.; Schnabel, Guido; Bryson, Patricia K.; Holmes, Gerald J. (2019).
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Petrasch, Stefan; Knapp, Steven J.; van Kan, Jan A. L.; Blanco-Ulate, Barbara (2019-04-04).
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Except where otherwise noted, data are given for materials in their
107: 97: 209: 661:"Within-Season Shift in Fungicide Resistance Profiles of 512:liquid chromatography–tandem mass spectrometry". 171: 83: 8: 224: 149: 127: 15: 686: 633: 191: 450: 273:COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC 270: 245: 220: 425:used on tree, vine, and root crops. 354:172 Â°C (342 Â°F; 445 K) 140: 252:Key: QGHREAKMXXNCOA-UHFFFAOYSA-N 7: 606:British Society for Plant Pathology 162: 679:American Phytopathological Society 464:. Environmental Protection Agency. 14: 62:-phenylene)bis(3-thioallophanate) 665:in California Strawberry Fields" 306: 300: 22: 376:(at 25 Â°C , 100 kPa). 318: 312: 294: 1: 562:10.1016/j.chroma.2016.01.045 526:10.1016/j.chroma.2011.01.034 550:Journal of Chromatography A 514:Journal of Chromatography A 767: 688:10.1094/pdis-03-18-0406-re 597:Molecular Plant Pathology 370: 281: 261: 236: 67: 55: 35: 30: 21: 435:strawberry in California 548:poisoning incidents". 421:. It is a widely used 478:Analytical Chemistry 459:"Thiophanate-methyl" 37:Preferred IUPAC name 361:Solubility in water 336: g·mol 18: 17:Thiophanate-methyl 398:with the formula C 392:Thiophanate-methyl 380:Infobox references 16: 618:10.1111/mpp.12794 520:(11): 1477–1485. 490:10.1021/ac801557f 484:(24): 9450–9459. 419:-phenylenediamine 388:Chemical compound 386: 385: 205:CompTox Dashboard 109:Interactive image 758: 720: 716: 690: 663:Botrytis cinerea 655: 637: 590:Botrytis cinerea 580: 574: 573: 544: 538: 537: 508: 502: 501: 472: 466: 465: 463: 455: 431:Botrytis cinerea 406:(NHC(S)NH(CO)OCH 396:organic compound 335: 320: 314: 308: 302: 296: 289:Chemical formula 229: 228: 213: 211: 195: 175: 164: 153: 142: 131: 111: 87: 26: 19: 766: 765: 761: 760: 759: 757: 756: 755: 726: 725: 724: 723: 719: 658: 585: 581: 577: 546: 545: 541: 510: 509: 505: 474: 473: 469: 461: 457: 456: 452: 447: 413: 409: 405: 401: 389: 382: 377: 363: 333: 323: 317: 311: 305: 299: 291: 277: 274: 269: 268: 257: 254: 253: 250: 244: 243: 232: 214: 207: 198: 178: 165: 134: 114: 101: 90: 77: 63: 58:Dimethyl 4,4′-( 51: 50: 12: 11: 5: 764: 762: 754: 753: 748: 743: 738: 728: 727: 722: 721: 718: 717: 656: 582: 575: 539: 503: 467: 449: 448: 446: 443: 411: 407: 403: 399: 387: 384: 383: 378: 374:standard state 371: 368: 367: 364: 359: 356: 355: 352: 346: 345: 342: 338: 337: 331: 325: 324: 321: 315: 309: 303: 297: 292: 287: 284: 283: 279: 278: 276: 275: 272: 264: 263: 262: 259: 258: 256: 255: 251: 248: 247: 239: 238: 237: 234: 233: 231: 230: 217: 215: 203: 200: 199: 197: 196: 188: 186: 180: 179: 177: 176: 168: 166: 158: 155: 154: 144: 136: 135: 133: 132: 124: 122: 116: 115: 113: 112: 104: 102: 95: 92: 91: 89: 88: 80: 78: 73: 70: 69: 65: 64: 57: 53: 52: 40: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 763: 752: 751:Methyl esters 749: 747: 744: 742: 739: 737: 734: 733: 731: 714: 710: 706: 702: 698: 694: 689: 684: 680: 676: 672: 671: 670:Plant Disease 666: 664: 657: 653: 649: 645: 641: 636: 631: 627: 623: 619: 615: 611: 607: 603: 599: 598: 593: 591: 584: 583: 579: 576: 571: 567: 563: 559: 555: 551: 543: 540: 535: 531: 527: 523: 519: 515: 507: 504: 499: 495: 491: 487: 483: 479: 471: 468: 460: 454: 451: 444: 442: 440: 436: 433: 432: 426: 424: 420: 418: 397: 393: 381: 375: 369: 365: 362: 358: 357: 353: 351: 350:Melting point 348: 347: 344:white powder 343: 340: 339: 332: 330: 327: 326: 293: 290: 286: 285: 280: 271: 267: 260: 246: 242: 235: 227: 223: 222:DTXSID1024338 219: 218: 216: 206: 202: 201: 194: 190: 189: 187: 185: 182: 181: 174: 170: 169: 167: 161: 157: 156: 152: 148: 145: 143: 141:ECHA InfoCard 138: 137: 130: 126: 125: 123: 121: 118: 117: 110: 106: 105: 103: 99: 94: 93: 86: 82: 81: 79: 76: 72: 71: 66: 61: 54: 49:′-dicarbamate 48: 44: 38: 34: 29: 25: 20: 674: 668: 662: 612:): 877–892. 601: 595: 589: 578: 553: 549: 542: 517: 513: 506: 481: 477: 470: 453: 429: 427: 416: 391: 390: 68:Identifiers 59: 56:Other names 46: 42: 556:: 100–114. 439:carbendazim 341:Appearance 282:Properties 147:100.041.567 746:Carbamates 736:Fungicides 730:Categories 445:References 366:26.6 mg/L 329:Molar mass 193:K4N81R84L8 120:ChemSpider 96:3D model ( 85:23564-05-8 75:CAS Number 741:Thioureas 713:205345358 697:0191-2917 681:: 59–64. 626:1464-6722 423:fungicide 41:Dimethyl 705:30422743 652:93002697 644:30945788 570:26830634 534:21292276 498:19072261 635:6637890 173:3032791 160:PubChem 129:2297683 711:  703:  695:  650:  642:  632:  624:  568:  532:  496:  394:is an 334:342.39 266:SMILES 31:Names 709:S2CID 677:(1). 648:S2CID 604:(6). 462:(PDF) 241:InChI 98:JSmol 701:PMID 693:ISSN 640:PMID 622:ISSN 566:PMID 554:1435 530:PMID 518:1218 494:PMID 184:UNII 683:doi 675:103 630:PMC 614:doi 610:W-B 558:doi 522:doi 486:doi 210:EPA 163:CID 732:: 707:. 699:. 691:. 673:. 667:. 646:. 638:. 628:. 620:. 602:20 600:. 594:. 564:. 552:. 528:. 516:. 492:. 482:80 480:. 441:. 304:14 298:12 715:. 685:: 654:. 616:: 608:( 592:" 572:. 560:: 536:. 524:: 500:. 488:: 417:o 412:2 410:) 408:3 404:4 402:H 400:6 322:2 319:S 316:4 313:O 310:4 307:N 301:H 295:C 212:) 208:( 100:) 60:o 47:N 45:, 43:N

Index

Chemical structure of thiophanate-methyl.
Preferred IUPAC name
CAS Number
23564-05-8
JSmol
Interactive image
ChemSpider
2297683
ECHA InfoCard
100.041.567
Edit this at Wikidata
PubChem
3032791
UNII
K4N81R84L8
CompTox Dashboard
DTXSID1024338
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
Melting point
Solubility in water
standard state
Infobox references
organic compound
o-phenylenediamine
fungicide
Botrytis cinerea

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