Home > Name List By 3 > 3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one

CAS No 60-82-2 , 3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one

  • Name: 3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one
  • Synonyms: Phloretol; 60-82-2; 3-(4-Hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one;3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one;Dihydronaringenin;
  • CAS Registry Number:
  • Melting Point: 260-262 ºC
  • Density: 1.429 g/cm3
  • Refractive index: 1.573-1.575
  • Safety Statements: R36/37/38
  • Hazard Symbols: Xi: Irritant;
  • EINECS: 200-488-7
  • Molecular Weight: 274.26866
  • InchiKey: VGEREEWJJVICBM-UHFFFAOYSA-N
  • InChI: InChI=1S/C15H14O5/c16-10-4-1-9(2-5-10)3-6-12(18)15-13(19)7-11(17)8-14
    (15)20/h1-2,4-5,7-8,16-17,19-20H,3,6H2
  • Risk Statements: S26;S37/39
  • Molecular Formula: C15H14O5
  • Molecular Structure:CAS No:60-82-2 3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one

Related products

Search by region :

Select to

60-82-2 Phloretin

Contact Supplier

Select to

4/4
Previous 1 2 3 4
References of 3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one
Title: Phloretin
CAS Registry Number: 60-82-2
CAS Name: 3-(4-Hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)-1-propanone
Synonyms: 2￠,4￠,6￠-trihydroxy-3-(p-hydroxyphenyl)propiophenone; b-(p-hydroxyphenyl)phloropropiophenone; b-(p-hydroxyphenyl)-2,4,6-trihydroxypropiophenone
Molecular Formula: C15H14O5
Molecular Weight: 274.27
Percent Composition: C 65.69%, H 5.14%, O 29.17%
Literature References: The aglucon of phlorizin, q.v. From root bark of apple trees: Rochleder, J. Prakt. Chem. 98, 205 (1866). Structure: Seshadri, Annu. Rev. Biochem. 20, 495 (1951). Synthesis: Fischer, Nouri, Ber. 50, 611 (1917); Rosenmund, Rosenmund, ibid. 61B, 2608 (1928); Shinoda et al., J. Pharm. Soc. Jpn. 49, 797 (1929); Johnston, US 2789995 (1957 to Union Carbide).
Properties: Needles from dil alcohol, dec 262°. Absorption spectrum: Lambrechts, Arch. Int. Physiol. 44, Suppl., 1-39 (1937). Freely sol in alc, methanol, acetone; sol in alkalies in hot glacial acetic acid; very sparingly sol in benzene, chloroform. Practically insol in water, ether, the soly being increased by addition of alcohol.