Knowledge (XXG)

Paracoumaryl alcohol

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258: 24: 392: 405: 515: 307: 610: 272: 412: 215: 236: 603: 99: 139: 681: 36: 253: 596: 459: 65: 575: 534:
Withers, Saunia; Lu, Fachuang; Kim, Hoon; Zhu, Yimin; Ralph, John; Wilkerson, Curtis G. (2012).
53:-coumaryl alcohol, 4-coumaryl alcohol, 4-hydroxycinnamyl alcohol, 4-(3-hydroxy-1-propenyl)phenol 634: 567: 159: 557: 547: 330: 224: 75: 639: 456: 257: 119: 562: 535: 383: 675: 428: 371: 579: 536:"Identification of Grass-specific Enzyme That Acylates Monolignols with p-Coumarate" 204: 491: 23: 620: 499: 473: 432: 353: 150: 660: 552: 571: 503: 495: 588: 191: 444: 440: 130: 382:
Except where otherwise noted, data are given for materials in their
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InChI=1S/C9H10O2/c10-7-1-2-8-3-5-9(11)6-4-8/h1-6,10-11H,7H2/b2-1+
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InChI=1/C9H10O2/c10-7-1-2-8-3-5-9(11)6-4-8/h1-6,10-11H,7H2/b2-1+
170: 592: 477: 241: 400: 653: 627: 376:114–116 °C (237–241 °F; 387–389 K) 203: 74: 604: 8: 611: 597: 589: 439:-Coumaryl alcohol is a major precursor to 256: 158: 15: 561: 551: 223: 516:Molecule of the week: p-coumaryl alcohol 490:-Coumaryl alcohol is an intermediate in 526: 312: 277: 252: 284:Key: PTNLHDGQWUGONS-OWOJBTEDSA-N 138: 118: 7: 294:Key: PTNLHDGQWUGONS-OWOJBTEDBL 194: 178: 14: 390: 22: 540:Journal of Biological Chemistry 386:(at 25 °C , 100 kPa). 476:are the basis of epicuticular 1: 451:Biosynthesis and occurrence 698: 455:It is synthesized via the 480:covering the surfaces of 380: 323: 303: 268: 58: 47: 35: 30: 21: 553:10.1074/jbc.M111.284497 435:. It is a white solid. 472:-coumaryl alcohol and 358:150.1745 17:Paracoumaryl alcohol 645:paracoumaryl alcohol 425:Paracoumaryl alcohol 37:Preferred IUPAC name 460:biochemical pathway 18: 413:Infobox references 315:OC/C=C/c1ccc(O)cc1 16: 669: 668: 635:coniferyl alcohol 546:(11): 8347–8355. 421:Chemical compound 419: 418: 237:CompTox Dashboard 100:Interactive image 689: 613: 606: 599: 590: 584: 583: 565: 555: 531: 403: 397: 394: 393: 331:Chemical formula 261: 260: 245: 243: 227: 207: 196: 182: 162: 142: 122: 102: 78: 26: 19: 697: 696: 692: 691: 690: 688: 687: 686: 672: 671: 670: 665: 649: 640:sinapyl alcohol 623: 617: 587: 533: 532: 528: 524: 512: 457:phenylpropanoid 453: 422: 415: 410: 409: 408:  ?) 399: 395: 391: 387: 347: 343: 339: 333: 319: 316: 311: 310: 299: 296: 295: 292: 286: 285: 282: 276: 275: 264: 246: 239: 230: 210: 197: 185: 165: 145: 125: 105: 92: 81: 68: 54: 43: 42: 12: 11: 5: 695: 693: 685: 684: 674: 673: 667: 666: 664: 663: 657: 655: 651: 650: 648: 647: 642: 637: 631: 629: 625: 624: 618: 616: 615: 608: 601: 593: 586: 585: 525: 523: 520: 519: 518: 511: 510:External links 508: 452: 449: 420: 417: 416: 411: 389: 388: 384:standard state 381: 378: 377: 374: 368: 367: 364: 360: 359: 356: 350: 349: 345: 341: 337: 334: 329: 326: 325: 321: 320: 318: 317: 314: 306: 305: 304: 301: 300: 298: 297: 293: 290: 289: 287: 283: 280: 279: 271: 270: 269: 266: 265: 263: 262: 254:DTXSID50895024 249: 247: 235: 232: 231: 229: 228: 220: 218: 212: 211: 209: 208: 200: 198: 190: 187: 186: 184: 183: 175: 173: 167: 166: 164: 163: 155: 153: 147: 146: 144: 143: 135: 133: 127: 126: 124: 123: 115: 113: 107: 106: 104: 103: 95: 93: 86: 83: 82: 80: 79: 71: 69: 64: 61: 60: 56: 55: 49: 45: 44: 40: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 694: 683: 680: 679: 677: 662: 659: 658: 656: 652: 646: 643: 641: 638: 636: 633: 632: 630: 626: 622: 614: 609: 607: 602: 600: 595: 594: 591: 581: 577: 573: 569: 564: 559: 554: 549: 545: 541: 537: 530: 527: 521: 517: 514: 513: 509: 507: 505: 501: 497: 493: 489: 485: 483: 479: 475: 471: 467: 463: 461: 458: 450: 448: 446: 442: 438: 434: 431:, one of the 430: 429:phytochemical 426: 414: 407: 402: 385: 379: 375: 373: 372:Melting point 370: 369: 365: 362: 361: 357: 355: 352: 351: 335: 332: 328: 327: 322: 313: 309: 302: 288: 278: 274: 267: 259: 255: 251: 250: 248: 238: 234: 233: 226: 222: 221: 219: 217: 214: 213: 206: 202: 201: 199: 193: 189: 188: 181: 177: 176: 174: 172: 169: 168: 161: 157: 156: 154: 152: 149: 148: 141: 137: 136: 134: 132: 129: 128: 121: 117: 116: 114: 112: 109: 108: 101: 97: 96: 94: 90: 85: 84: 77: 73: 72: 70: 67: 63: 62: 57: 52: 46: 38: 34: 29: 25: 20: 644: 543: 539: 529: 492:biosynthesis 487: 486: 469: 464: 454: 436: 424: 423: 366:White solid 140:ChEMBL109034 59:Identifiers 50: 48:Other names 682:Monolignols 621:monolignols 500:stilbenoids 474:fatty acids 433:monolignols 363:Appearance 324:Properties 120:CHEBI:64555 654:Glycosides 522:References 354:Molar mass 225:61POZ1QQ11 151:ChemSpider 87:3D model ( 76:20649-40-5 66:CAS Number 661:Coniferin 628:Aglycones 619:Types of 676:Category 580:24998478 572:22267741 504:coumarin 496:chavicol 41:4-phenol 563:3318722 445:lignans 406:what is 404: ( 348: 205:5280535 192:PubChem 160:4444166 578:  570:  560:  502:, and 482:apples 466:Esters 441:lignin 401:verify 398:  308:SMILES 180:C02646 131:ChEMBL 31:Names 576:S2CID 478:waxes 427:is a 273:InChI 111:ChEBI 89:JSmol 568:PMID 216:UNII 171:KEGG 558:PMC 548:doi 544:287 494:of 468:of 462:. 443:or 242:EPA 195:CID 678:: 574:. 566:. 556:. 542:. 538:. 506:. 498:, 484:. 447:. 342:10 612:e 605:t 598:v 582:. 550:: 488:p 470:p 437:p 396:N 346:2 344:O 340:H 338:9 336:C 244:) 240:( 91:) 51:p

Index


Preferred IUPAC name
CAS Number
20649-40-5
JSmol
Interactive image
ChEBI
CHEBI:64555
ChEMBL
ChEMBL109034
ChemSpider
4444166
KEGG
C02646
PubChem
5280535
UNII
61POZ1QQ11
CompTox Dashboard
DTXSID50895024
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
Melting point
standard state
verify
what is
Infobox references

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