Tyrosinol

Source: Wikipedia, the free encyclopedia.
Tyrosinol
Names
Other names
β-amino-4-hydroxybenzenepropanol
Identifiers
3D model (
JSmol
)
ChemSpider
  • InChI=1S/C9H13NO2/c10-8(6-11)5-7-1-3-9(12)4-2-7/h1-4,8,11-12H,5-6,10H2
    Key: DBLDQZASZZMNSL-UHFFFAOYSA-N
  • (L-): InChI=1S/C9H13NO2/c10-8(6-11)5-7-1-3-9(12)4-2-7/h1-4,8,11-12H,5-6,10H2/t8-/m0/s1
    Key: DBLDQZASZZMNSL-QMMMGPOBSA-N
  • (D-): InChI=1S/C9H13NO2/c10-8(6-11)5-7-1-3-9(12)4-2-7/h1-4,8,11-12H,5-6,10H2/t8-/m1/s1
    Key: DBLDQZASZZMNSL-MRVPVSSYSA-N
  • C(C(CO)N)C1=CC=C(O)C=C1
  • (L-): C1=CC(=CC=C1C[C@@H](CO)N)O
  • (D-): C1=CC(=CC=C1C[C@H](CO)N)O
Properties
C9H13NO2
Molar mass 167.208 g·mol−1
Appearance white solid
Melting point 91.4–92.1 °C (196.5–197.8 °F; 364.5–365.2 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Tyrosinol is an

chiral, is an example of a 1,2-ethanolamine as well as a phenethylamine.[2]

Related compounds

References