Knowledge (XXG)

Flusilazole

Source 📝

247: 172: 33: 678: 24: 399: 412: 540:"Effects of fungicides on in vitro spore germination and mycelial growth of the phytopathogens Leptosphaeria maculans and L. biglobosa (phoma stem canker of oilseed rape)" 719: 503:
Bostanian NJ, Larocque N, Chouinard G, Coderre D (November 2001). "Baseline toxicity of several pesticides to Hyaliodes vitripennis (Say) (Hemiptera: Miridae)".
296: 109: 616:"Relative embryotoxicity of two classes of chemicals in a modified zebrafish embryotoxicity test and comparison with their in vivo potencies" 712: 753: 487: 261: 743: 758: 579:
Farag AT, Ibrahim HH (February 2007). "Developmental toxic effects of antifungal flusilazole administered by gavage to mice".
705: 419: 204: 225: 449:, which is used to control fungal infections on a variety of fruit and vegetable crops. It is moderately toxic to 748: 470:
Moberg, W. K.; Basarab, G. S.; Cuomo, J.; Liang, P. H. (1987). "Biologically Active Organosilicon Compounds".
167: 270:
InChI=1S/C16H15F2N3Si/c1-22(12-21-11-19-10-20-21,15-6-2-13(17)3-7-15)16-8-4-14(18)5-9-16/h2-11H,12H2,1H3
280:
InChI=1/C16H15F2N3Si/c1-22(12-21-11-19-10-20-21,15-6-2-13(17)3-7-15)16-8-4-14(18)5-9-16/h2-11H,12H2,1H3
45: 738: 620: 242: 75: 639: 596: 561: 520: 483: 689: 685: 629: 588: 551: 512: 475: 377: 319: 213: 149: 85: 661: 246: 171: 129: 390: 732: 439: 366: 160: 32: 193: 677: 479: 634: 615: 346: 140: 614:
Hermsen SA, van den Brandhof EJ, van der Ven LT, Piersma AH (January 2011).
442: 643: 600: 565: 524: 581:
Birth Defects Research Part B: Developmental and Reproductive Toxicology
23: 592: 356: 180: 450: 446: 556: 539: 389:
Except where otherwise noted, data are given for materials in their
516: 120: 108: 98: 230: 453:
and has been shown to produce birth defects in high doses.
474:. ACS Symposium Series. Vol. 355. pp. 288–301. 693: 407: 538:
Eckert MR, Rossall S, Selley A, Fitt BD (April 2010).
192: 84: 713: 8: 665:in the Pesticide Properties DataBase (PPDB) 720: 706: 245: 170: 148: 15: 633: 555: 212: 472:Synthesis and Chemistry of Agrochemicals 462: 301: 266: 241: 161: 273:Key: FQKUGOMFVDPBIZ-UHFFFAOYSA-N 128: 7: 674: 672: 304:c2ncnn2C(C)(c(cc1)ccc1F)c3ccc(F)cc3 283:Key: FQKUGOMFVDPBIZ-UHFFFAOYAI 183: 692:. You can help Knowledge (XXG) by 14: 676: 397: 31: 22: 393:(at 25 °C , 100 kPa). 1: 351:315.392 g/mol 775: 671: 480:10.1021/bk-1987-0355.ch026 635:10.1016/j.tiv.2011.01.005 387: 312: 292: 257: 68: 60: 44: 39: 30: 21: 754:4-Fluorophenyl compounds 744:Organosilicon compounds 544:Pest Management Science 505:Pest Management Science 759:Organic compound stubs 684:This article about an 46:Preferred IUPAC name 621:Toxicology in Vitro 378:Solubility in water 18: 593:10.1002/bdrb.20098 420:Infobox references 16: 701: 700: 428:Chemical compound 426: 425: 383:41.9 mg/L (20°C) 226:CompTox Dashboard 110:Interactive image 766: 722: 715: 708: 686:organic compound 680: 673: 648: 647: 637: 611: 605: 604: 576: 570: 569: 559: 535: 529: 528: 500: 494: 493: 467: 410: 404: 401: 400: 320:Chemical formula 250: 249: 234: 232: 216: 196: 185: 174: 163: 152: 132: 112: 88: 35: 26: 19: 774: 773: 769: 768: 767: 765: 764: 763: 749:Embryotoxicants 729: 728: 727: 726: 669: 657: 652: 651: 613: 612: 608: 578: 577: 573: 557:10.1002/ps.1890 537: 536: 532: 511:(11): 1007–10. 502: 501: 497: 490: 469: 468: 464: 459: 429: 422: 417: 416: 415:  ?) 406: 402: 398: 394: 380: 340: 336: 332: 328: 322: 308: 305: 300: 299: 288: 285: 284: 281: 275: 274: 271: 265: 264: 253: 235: 228: 219: 199: 186: 155: 135: 115: 102: 91: 78: 64: 56: 55: 54:-1,2,4-triazole 12: 11: 5: 772: 770: 762: 761: 756: 751: 746: 741: 731: 730: 725: 724: 717: 710: 702: 699: 698: 681: 667: 666: 656: 655:External links 653: 650: 649: 628:(3): 745–753. 606: 571: 550:(4): 396–405. 530: 517:10.1002/ps.374 495: 488: 461: 460: 458: 455: 427: 424: 423: 418: 396: 395: 391:standard state 388: 385: 384: 381: 376: 373: 372: 369: 363: 362: 359: 353: 352: 349: 343: 342: 338: 334: 330: 326: 323: 318: 315: 314: 310: 309: 307: 306: 303: 295: 294: 293: 290: 289: 287: 286: 282: 279: 278: 276: 272: 269: 268: 260: 259: 258: 255: 254: 252: 251: 238: 236: 224: 221: 220: 218: 217: 209: 207: 201: 200: 198: 197: 189: 187: 179: 176: 175: 165: 157: 156: 154: 153: 145: 143: 137: 136: 134: 133: 125: 123: 117: 116: 114: 113: 105: 103: 96: 93: 92: 90: 89: 81: 79: 74: 71: 70: 66: 65: 62: 58: 57: 49: 48: 42: 41: 37: 36: 28: 27: 13: 10: 9: 6: 4: 3: 2: 771: 760: 757: 755: 752: 750: 747: 745: 742: 740: 737: 736: 734: 723: 718: 716: 711: 709: 704: 703: 697: 695: 691: 687: 682: 679: 675: 670: 664: 663: 659: 658: 654: 645: 641: 636: 631: 627: 623: 622: 617: 610: 607: 602: 598: 594: 590: 586: 582: 575: 572: 567: 563: 558: 553: 549: 545: 541: 534: 531: 526: 522: 518: 514: 510: 506: 499: 496: 491: 489:9780841214347 485: 481: 477: 473: 466: 463: 456: 454: 452: 448: 444: 441: 440:organosilicon 437: 433: 421: 414: 409: 392: 386: 382: 379: 375: 374: 370: 368: 367:Melting point 365: 364: 360: 358: 355: 354: 350: 348: 345: 344: 324: 321: 317: 316: 311: 302: 298: 291: 277: 267: 263: 256: 248: 244: 243:DTXSID3024235 240: 239: 237: 227: 223: 222: 215: 211: 210: 208: 206: 203: 202: 195: 191: 190: 188: 182: 178: 177: 173: 169: 166: 164: 162:ECHA InfoCard 159: 158: 151: 147: 146: 144: 142: 139: 138: 131: 127: 126: 124: 122: 119: 118: 111: 107: 106: 104: 100: 95: 94: 87: 83: 82: 80: 77: 73: 72: 67: 59: 53: 47: 43: 38: 34: 29: 25: 20: 694:expanding it 683: 668: 660: 625: 619: 609: 584: 580: 574: 547: 543: 533: 508: 504: 498: 471: 465: 445:invented by 435: 431: 430: 69:Identifiers 61:Other names 51: 50:1-{methyl}-1 17:Flusilazole 662:Flusilazole 587:(1): 12–7. 432:Flusilazole 313:Properties 168:100.107.525 130:CHEBI:81922 739:Fungicides 733:Categories 457:References 371:53–55 °C[ 361:1.31 g/cm 347:Molar mass 214:F3WG2VVD87 141:ChemSpider 97:3D model ( 86:85509-19-9 76:CAS Number 63:DPX-H6573; 443:fungicide 436:DPX-H6573 341:Si 644:21238576 601:17187383 566:20013877 525:11721516 438:) is an 451:animals 413:what is 411: ( 357:Density 181:PubChem 642:  599:  564:  523:  486:  447:DuPont 408:verify 405:  297:SMILES 40:Names 688:is a 262:InChI 194:73675 150:66326 121:ChEBI 99:JSmol 690:stub 640:PMID 597:PMID 562:PMID 521:PMID 484:ISBN 205:UNII 630:doi 589:doi 552:doi 513:doi 476:doi 231:EPA 184:CID 735:: 638:. 626:25 624:. 618:. 595:. 585:80 583:. 560:. 548:66 546:. 542:. 519:. 509:57 507:. 482:. 331:15 327:16 721:e 714:t 707:v 696:. 646:. 632:: 603:. 591:: 568:. 554:: 527:. 515:: 492:. 478:: 434:( 403:N 339:3 337:N 335:2 333:F 329:H 325:C 233:) 229:( 101:) 52:H

Index



Preferred IUPAC name
CAS Number
85509-19-9
JSmol
Interactive image
ChEBI
CHEBI:81922
ChemSpider
66326
ECHA InfoCard
100.107.525
Edit this at Wikidata
PubChem
73675
UNII
F3WG2VVD87
CompTox Dashboard
DTXSID3024235
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
Density
Melting point
Solubility in water
standard state
verify

Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.