Skip to main content

  | मौसम…

411 समाचार
Public archive edition · Attributed source reporting with original dates · AI drafts are excluded

411 REFERENCE · Wikipedia

2,4-Dihydroxybenzoic acid

Reference material by Wikipedia contributors. This retains its source identity and is not 411 news reporting.

changed 477198363 2,4-Dihydroxybenzoic acid 2,4-Dihydroxybenzoesäure.svg 100px Chemical structure of 2,4-dihydroxybenzoic acid Chemical structure of 2,4-dihydroxybenzoic acid 2,4-Dihydroxybenzoic acid β-Resorcylic acidβ-Resorcinolic acid p-Hydroxysalicylic acid 2,4-DHBA 89-86-1 correct CAS correct FDA LU39SC9JYL correct EBI 328910 42094 1491 correct chemspider 1446 correct drugbank DB02839 correct chemspider 1S/C7H6O4/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,8-9H,(H,10,11) correct chemspider UIAFKZKHHVMJGS-UHFFFAOYSA-N C1=CC(=C(C=C1O)O)C(=O)O Haynes, William M. 2016 CRC Handbook of Chemistry and Physics 97th CRC Press 3 190 https://ia800704.us.archive.org/27/items/CRCHandbookOfChemistryAndPhysics97thEdition2016/CRC%20Handbook%20of%20Chemistry%20and%20Physics%20-%2097th%20Edition%20%282016%29.pdf?page=3-190 9781498754293 7 6 4 229 soluble soluble ethanol soluble diethyl ether soluble benzene 3.11 8.55 14.0Haynes, William M. 2016 CRC Handbook of Chemistry and Physics 97th CRC Press 5 91 https://ia800704.us.archive.org/27/items/CRCHandbookOfChemistryAndPhysics97thEdition2016/CRC%20Handbook%20of%20Chemistry%20and%20Physics%20-%2097th%20Edition%20%282016%29.pdf?page=5-91 9781498754293 07 warning 315 319 335 261 280 302+352 305+351+338 GHS: GESTIS 492493 2,3-Dihydroxybenzoic acid 2,5-Dihydroxybenzoic acid 2,6-Dihydroxybenzoic acid 3,4-Dihydroxybenzoic acid 3,5-Dihydroxybenzoic acid 2,4-Dihydroxybenzoic acid (β-resorcylic acid) is a dihydroxybenzoic acid. As a resorcylic acid, it is one of the three isomeric crystalline acids that are both carboxyl derivatives of resorcinol and dihydroxy derivatives of benzoic acid. Synthesis from resorcinol is via the Kolbe-Schmitt reaction.Organikum: organisch-chemisches Grundpraktikum Johann Ambrosius Barth 1993 978-3-335-00343-4 Becker Heinz G.O. 19th (rev. and expanded) Leipzig 351–352 German It is a degradation product of cyanidin glycosides from tart cherries in cell cultures.10.1021/jf0107508 Degradation Products of Cyanidin Glycosides from Tart Cherries and Their Bioactivities 2001 Seeram Navindra P. Bourquin Leslie D. Nair Muraleedharan G. Journal of Agricultural and Food Chemistry 49 10 4924–4929 11600045 It is also a metabolite found in human plasma after cranberry juice consumption.10.1021/jf035073r GC-MS Determination of Flavonoids and Phenolic and Benzoic Acids in Human Plasma after Consumption of Cranberry Juice 2004 Zhang Kai Zuo Yuegang Journal of Agricultural and Food Chemistry 52 2 222–227 14733499 References Category:Dihydroxybenzoic acids