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Rosarin

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Mudge, E.; Lopes-Lutz, D.; Brown, P. N.; Schieber, A. (2013). "Purification of Phenylalkanoids and monoterpene glycosides from Rhodiola rosea L. Roots by high-speed counter-current chromatography".
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InChI=1S/C20H28O10/c21-9-12-14(22)17(25)20(29-12)28-10-13-15(23)16(24)18(26)19(30-13)27-8-4-7-11-5-2-1-3-6-11/h1-7,12-26H,8-10H2/b7-4+/t12-,13+,14-,15+,16-,17+,18+,19+,20+/m0/s1
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InChI=1/C20H28O10/c21-9-12-14(22)17(25)20(29-12)28-10-13-15(23)16(24)18(26)19(30-13)27-8-4-7-11-5-2-1-3-6-11/h1-7,12-26H,8-10H2/b7-4+/t12-,13+,14-,15+,16-,17+,18+,19+,20+/m0/s1
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Except where otherwise noted, data are given for materials in their
118: 224: 214: 15: 307: 39: 540: 43: 381:C1=CC=C(C=C1)/C=C/CO2((((O2)CO3(((O3)CO)O)O)O)O)O 269: 200: 560: 8: 48:introducing citations to additional sources 567: 553: 322: 244: 178:)-2-({oxy}methyl)-6-{oxy}oxane-3,4,5-triol 110: 289: 38:Relevant discussion may be found on the 479: 378: 343: 318: 350:Key: IEBFEMIXXHIISM-YZOUKVLTSA-N 7: 521: 519: 360:Key: IEBFEMIXXHIISM-YZOUKVLTBR 260: 14: 523: 408: 117: 31:relies largely or entirely on a 20: 442:(at 25 °C , 100 kPa). 414: 402: 1: 539:. You can help Knowledge by 139:)-3-Phenylprop-2-en-1-yl α- 607: 586:Phenylpropanoid glycosides 518: 143:-arabinofuranosyl-(1→6)-β- 436: 389: 369: 334: 184: 152: 130: 125: 116: 464:glycoside isolated from 591:Organic compound stubs 531:This article about an 489:Phytochemical Analysis 154:Systematic IUPAC name 44:improve this article 432: g·mol 113: 446:Infobox references 111: 548: 547: 454:Chemical compound 452: 451: 303:CompTox Dashboard 226:Interactive image 146: 142: 109: 108: 94: 598: 569: 562: 555: 533:organic compound 527: 520: 513: 512: 501:10.1002/pca.2391 484: 462:cinnamyl alcohol 431: 416: 410: 404: 397:Chemical formula 327: 326: 311: 309: 293: 273: 262: 248: 228: 204: 147:-glucopyranoside 144: 140: 121: 114: 104: 101: 95: 93: 52: 24: 16: 606: 605: 601: 600: 599: 597: 596: 595: 576: 575: 574: 573: 517: 516: 486: 485: 481: 476: 455: 448: 443: 429: 419: 413: 407: 399: 385: 382: 377: 376: 365: 362: 361: 358: 352: 351: 348: 342: 341: 330: 320:DTXSID601045580 312: 305: 296: 276: 263: 251: 231: 218: 207: 194: 180: 179: 148: 105: 99: 96: 53: 51: 37: 25: 12: 11: 5: 604: 602: 594: 593: 588: 578: 577: 572: 571: 564: 557: 549: 546: 545: 528: 515: 514: 495:(2): 129–134. 478: 477: 475: 472: 467:Rhodiola rosea 453: 450: 449: 444: 440:standard state 437: 434: 433: 427: 421: 420: 417: 411: 405: 400: 395: 392: 391: 387: 386: 384: 383: 380: 372: 371: 370: 367: 366: 364: 363: 359: 356: 355: 353: 349: 346: 345: 337: 336: 335: 332: 331: 329: 328: 315: 313: 301: 298: 297: 295: 294: 286: 284: 278: 277: 275: 274: 266: 264: 256: 253: 252: 250: 249: 241: 239: 233: 232: 230: 229: 221: 219: 212: 209: 208: 206: 205: 197: 195: 190: 187: 186: 182: 181: 157: 156: 150: 149: 134: 128: 127: 123: 122: 107: 106: 100:September 2014 42:. Please help 28: 26: 19: 13: 10: 9: 6: 4: 3: 2: 603: 592: 589: 587: 584: 583: 581: 570: 565: 563: 558: 556: 551: 550: 544: 542: 538: 534: 529: 526: 522: 510: 506: 502: 498: 494: 490: 483: 480: 473: 471: 469: 468: 463: 459: 447: 441: 435: 428: 426: 423: 422: 401: 398: 394: 393: 388: 379: 375: 368: 354: 344: 340: 333: 325: 321: 317: 316: 314: 304: 300: 299: 292: 288: 287: 285: 283: 280: 279: 272: 268: 267: 265: 259: 255: 254: 247: 243: 242: 240: 238: 235: 234: 227: 223: 222: 220: 216: 211: 210: 203: 199: 198: 196: 193: 189: 188: 183: 177: 173: 169: 165: 161: 155: 151: 138: 133: 129: 124: 120: 115: 103: 92: 89: 85: 82: 78: 75: 71: 68: 64: 61: –  60: 56: 55:Find sources: 49: 45: 41: 35: 34: 33:single source 29:This article 27: 23: 18: 17: 541:expanding it 530: 492: 488: 482: 465: 457: 456: 185:Identifiers 175: 171: 167: 163: 159: 136: 97: 87: 80: 73: 66: 54: 30: 390:Properties 580:Categories 474:References 425:Molar mass 291:PQA54L0KFI 237:ChemSpider 213:3D model ( 202:84954-93-8 192:CAS Number 132:IUPAC name 70:newspapers 59:"Rosarin" 40:talk page 509:22811209 271:10320370 112:Rosarin 458:Rosarin 430:428.434 258:PubChem 246:8495834 84:scholar 507:  374:SMILES 126:Names 86:  79:  72:  65:  57:  535:is a 460:is a 339:InChI 215:JSmol 91:JSTOR 77:books 537:stub 505:PMID 282:UNII 63:news 497:doi 308:EPA 261:CID 46:by 582:: 503:. 493:24 491:. 470:. 418:10 412:28 406:20 174:,6 170:,5 166:,4 162:,3 158:(2 135:(2 568:e 561:t 554:v 543:. 511:. 499:: 415:O 409:H 403:C 310:) 306:( 217:) 176:R 172:R 168:S 164:S 160:R 145:D 141:L 137:E 102:) 98:( 88:· 81:· 74:· 67:· 50:. 36:.

Index


single source
talk page
improve this article
introducing citations to additional sources
"Rosarin"
news
newspapers
books
scholar
JSTOR

IUPAC name
Systematic IUPAC name
CAS Number
84954-93-8
JSmol
Interactive image
ChemSpider
8495834
PubChem
10320370
UNII
PQA54L0KFI
CompTox Dashboard
DTXSID601045580
Edit this at Wikidata
InChI
SMILES
Chemical formula

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