CONTACT US
Home > Reference Standards> > Ethyl 3,5-dihydroxybenzoate
4142-98-7-Ethyl 3,5-dihydroxybenzoate Ethyl 3,5-dihydroxybenzoate

Ethyl 3,5-dihydroxybenzoate

For research use only. Not for therapeutic Use.

  • CAT Number: M001932
  • CAS Number: 4142-98-7
  • Molecular Formula: C9H10O4
  • Molecular Weight: 182.175
  • Purity: ≥95%
Inquiry Now
Related Small Molecules: 3-Amino-6-chloropyridine     4-Amino-1.8-naphthalic anhydride     Tributyl borate    

<p>
Ethyl 3,5-dihydroxybenzoate( CAS&nbsp;4142-98-7)&nbsp;<span style="font-size:12px;"><span style="font-family: Arial, Helvetica, sans-serif; font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;is a dihydroxybenzoic ester.</span><span style="font-family: Arial, Helvetica, sans-serif; font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;It can be synthesized from 3,5-dihydroxybenzoic acid by esterification process with absolute ethanol. It&nbsp;may be used as a starting reagent in the synthesis of ethyl 3,5-bis(&omega;-hydroxyoligo(et</span><wbr style="color: rgb(102, 94, 88); font-family: Arial, Helvetica, sans-serif; font-variant-ligatures: normal; orphans: 2; widows: 2;" /><span style="font-family: Arial, Helvetica, sans-serif; font-variant-ligatures: normal; orphans: 2; widows: 2;">hyleneoxy))benzoates</span><span style="font-family: Arial, Helvetica, sans-serif; font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;and <em>p</em></span><span style="font-family: Arial, Helvetica, sans-serif; font-variant-ligatures: normal; orphans: 2; widows: 2;">-alkoxycarbonylated palladium bis(phosphinite) PCP pincer complexes.</span></span></p>


Catalog Number M001932
CAS Number 4142-98-7
Synonyms

RARECHEM AL BI 0252;3,5-dihydroxybenzoicacidethylesterhemihydrate;alpha-resorcylicacid,ethylester,hemihydrate;benzoicacid,3,5-dihydroxy-,ethylester,hemihydrate;ethyl3,5-dihydroxybenzoatehemihydrate;ETHYL 3,5-DIHYDROXYBENZOATE;3,5-dihydroxybenzoic aci

Molecular Formula C9H10O4
Purity ≥95%
Storage Store at -20C
IUPAC Name ethyl 3,5-dihydroxybenzoate
InChI InChI=1S/C9H10O4/c1-2-13-9(12)6-3-7(10)5-8(11)4-6/h3-5,10-11H,2H2,1H3
InChIKey APHYVLPIZUVDTK-UHFFFAOYSA-N
SMILES CCOC(=O)C1=CC(=CC(=C1)O)O
Reference

1: Dong LM, Jia XC, Luo QW, Zhang Q, Luo B, Liu WB, Zhang X, Xu QL, Tan JW. Phenolics from Mikania micrantha and Their Antioxidant Activity. Molecules. 2017 Jul 8;22(7). pii: E1140. doi: 10.3390/molecules22071140. PubMed PMID: 28698451.<br />
2: Kwon BJ, Lee MH, Koo MA, Kim MS, Seon GM, Han JJ, Park JC. Ethyl-2, 5-dihydroxybenzoate displays dual activity by promoting osteoblast differentiation and inhibiting osteoclast differentiation. Biochem Biophys Res Commun. 2016 Mar 11;471(3):335-41. doi: 10.1016/j.bbrc.2016.02.017. Epub 2016 Feb 8. PubMed PMID: 26869515.<br />
3: Concepci&oacute;n RL, Froyl&aacute;n IV, Herminia I PM, Norberto MA, H&eacute;ctor J SZ, Yeniel GC. In vitro assessment of the acaricidal activity of computer-selected analogues of carvacrol and salicylic acid on Rhipicephalus (Boophilus) microplus. Exp Appl Acarol. 2013 Oct;61(2):251-7. doi: 10.1007/s10493-013-9688-4. Epub 2013 Apr 1. PubMed PMID: 23543288.<br />
4: Hopper DJ, Chapman PJ. Gentisic acid and its 3- and 4-methyl-substituted homologoues as intermediates in the bacterial degradation of m-cresol, 3,5-xylenol and 2,5-xylenol. Biochem J. 1971 Mar;122(1):19-28. PubMed PMID: 4330964; PubMed Central PMCID: PMC1176683.

Request a Quote