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Phloretic acid information


Phloretic acid
Chemical structure of phloretic acid
Names
Preferred IUPAC name
3-(4-Hydroxyphenyl)propanoic acid
Other names
Desaminotyrosine
Hydro-p-coumaric acid
Phloretate
Identifiers
CAS Number
  • 501-97-3 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:32980
ChemSpider
  • 9965
ECHA InfoCard 100.007.211 Edit this at Wikidata
EC Number
  • 207-931-3
KEGG
  • C01744
MeSH C008869
PubChem CID
  • 10394
UNII
  • 6QNC6P18SR checkY
CompTox Dashboard (EPA)
  • DTXSID2075427 Edit this at Wikidata
InChI
  • InChI=1S/C9H10O3/c10-8-4-1-7(2-5-8)3-6-9(11)12/h1-2,4-5,10H,3,6H2,(H,11,12)
    Key: NMHMNPHRMNGLLB-UHFFFAOYSA-N
SMILES
  • C1=CC(=CC=C1CCC(=O)O)O
Properties
Chemical formula
C9H10O3
Molar mass 166.176 g·mol−1
Melting point 129 °C (264 °F; 402 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Phloretic acid is an organic compound with the formula HOC6H4(CH2)2CO2H. It is a white solid. The compound contains both phenol and carboxylic acid functional groups. It is sometimes called Desaminotyrosine (DAT) because it is identical to the common alpha amino acid tyrosine except for the absence of the amino functional group on the alpha carbon.

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Phloretic acid

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Phloretic acid is an organic compound with the formula HOC6H4(CH2)2CO2H. It is a white solid. The compound contains both phenol and carboxylic acid functional...

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Phloroglucinol

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aqueous ammonia at low temperatures. Reaction of phloroglucinol and phloretic acid gives 30% yield of phloretin[citation needed]. Phloroglucinol is also...

Word Count : 1959

Tyrosine

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which in turn can be oxidized by the citric acid cycle or be used for fatty acid synthesis. Phloretic acid is also a urinary metabolite of tyrosine in...

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C9H10O3

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2-Ethoxybenzoic acid Ethylparaben Ethyl salicylate Ethylvanillin Methyl anisate Paeonol, a natural phenol Phloretic acid, a phenylpropanoid Tropic acid This set...

Word Count : 85

Phloretin

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the small intestine. Phloretin hydrolase hydrolyses phloretin into phloretic acid and phloroglucinol. In an animal model, phloretin inhibited active transport...

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Polymer stabilizer

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position of the phenol (i.e. they are ortho-alkylated analogues of phloretic acid). The quinone methides of these can rearrange once to give a hydroxycinnamate...

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