- 1,5-
Dihydroxynaphthalene is an
organic compound with the
formula C10H6(OH)2. It is one of
several isomers of
dihydroxynaphthalene. A
white solid, degraded...
- 1,2-
dihydroxynaphthalene dioxygenase (EC 1.13.11.56, 1,2-DHN dioxygenase, DHNDO, 1,2-
dihydroxynaphthalene oxygenase, 1,2-
dihydroxynaphthalene:oxygen oxidoreductase)...
- not
working near a
place where naphthalene production occurs. 1,2-
Dihydroxynaphthalene has been used as a
potential biomarker of
excessive exposure to naphthalene...
-
molecular formula C10H8O2 may
refer to: 1,5-
Dihydroxynaphthalene, one of
several isomers of
dihydroxynaphthalene Methylcoumarin,
isomer in
which a methyl...
-
Chromotropic acid
Names Preferred IUPAC name 4,5-
Dihydroxynaphthalene-2,7-disulfonic acid
Identifiers CAS
Number 148-25-4 Y 3D
model (JSmol) Interactive...
- Bucherer-Le
Petit reaction. The
reaction is used to
convert 1,7-
dihydroxynaphthalene into 7-amino-1-naphthol and 1-aminonaphthalene-4-sulfonic acid into...
-
created in 2012.
Genes were
identified that are
involved in the
dihydroxynaphthalene (DHN)-melanin
biosynthesis pathway which confirms the
etiology of...
- 1-nitronaphthalene. It can also be
prepared by
treatment of 1,5-
dihydroxynaphthalene with
ammonium sulfite. It is a
precursor to naphthalene-1,5-diisocyanate...
-
Fusion of Armstrong's acid in NaOH
gives the
disodium salt of 1,5-
dihydroxynaphthalene,
which can be
acidified to give the diol. The
intermediate in this...
- skin diseases.
Juglone is
derived by
oxidation of hydrojuglone, 1,5-
dihydroxynaphthalene,
after enzymatic hydrolysis. It can also be
obtained by oxidations...
