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Phthalazine

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Phthalazine Basic information

Product Name:
Phthalazine
Synonyms:
  • 2,3-Diazanaphthalene
  • beta-Phenodiazine
  • β-Phenodiazine
  • 4,5-BENZOPYRIDAZINE
  • 2,3-BENZODIAZINE
  • BENZO[D]PYRIDAZINE
  • PHTHALAZINE
  • PHZ
CAS:
253-52-1
MF:
C8H6N2
MW:
130.15
EINECS:
205-963-2
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • Pyridazines
Mol File:
253-52-1.mol
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Phthalazine Chemical Properties

Melting point:
89-92 °C(lit.)
Boiling point:
189 °C29 mm Hg(lit.)
Density 
1.1509 (rough estimate)
refractive index 
1.6231 (estimate)
Flash point:
178-180°C/15mm
storage temp. 
2-8°C
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Crystalline Powder
pka
3.47(at 20℃)
color 
Slightly brown to beige
Water Solubility 
Soluble in water, methanol, chloroform.
Merck 
14,7370
BRN 
109240
CAS DataBase Reference
253-52-1(CAS DataBase Reference)
NIST Chemistry Reference
Phthalazine(253-52-1)
EPA Substance Registry System
Phthalazine (253-52-1)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-68
Safety Statements 
24/25-37/39-36-26-36/37/39
WGK Germany 
3
TSCA 
Yes
HS Code 
29339900

MSDS

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Phthalazine Usage And Synthesis

Chemical Properties

SLIGHTLY BROWN TO BEIGE CRYSTALLINE POWDER

Uses

Phthalazine derivatives including copper and platinum complexes were induce the apoptosis in breast cancer cell lines and renal hyperemia.

Uses

Phthalazine is a heterocyclic organic compound isomeric with quinoxaline, cinnoline and quinazoline. Aminophthalazine compounds serve as effective phosphodiesterase (PDE) inhibitors.

Definition

ChEBI: Phthalazine is an azaarene that is the 2,3-diaza analogue of naphthalene. The parent of the class of phthalazines. It is a mancude organic heterobicyclic parent, a member of phthalazines, an azaarene and an ortho-fused heteroarene.

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 2, p. 206, 1965 DOI: 10.1002/jhet.5570020219

Purification Methods

Phthalazine crystallises from diethyl ether or *benzene, and sublimes under a vacuum. The hydrochloride forms needles from EtOH with m 235-236o(dec) and the picrate has m 208-210o. [Armarego J Appl Chem 11 70 1961, Beilstein 23 H 174, 23 III/IV 1233.]

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