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Key Documents

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P38706

Sigma-Aldrich

Phthalazine

98%

Sinónimos:

β-Phenodiazine, 2,3-Benzodiazine, 2,3-Diazanaphthalene, Benzo[d]pyridazine

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About This Item

Fórmula empírica (notación de Hill):
C8H6N2
Número de CAS:
253-52-1
Peso molecular:
130.15
EC Number:
205-963-2
MDL number:
MFCD00006908
UNSPSC Code:
12352100
PubChem Substance ID:
24898461
NACRES:
NA.22

assay

98%

form

crystals

bp

189 °C/29 mmHg (lit.)

mp

89-92 °C (lit.)

storage temp.

2-8°C

SMILES string

c1ccc2cnncc2c1

InChI

1S/C8H6N2/c1-2-4-8-6-10-9-5-7(8)3-1/h1-6H

InChI key

LFSXCDWNBUNEEM-UHFFFAOYSA-N

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pictograms

Health hazard
GHS08

signalword

Warning

hcodes

H341,H412

Hazard Classifications

Aquatic Chronic 3 - Muta. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Hyungchul Kim et al.
International journal of pharmaceutics, 377(1-2), 105-111 (2009-05-26)
Investigation of the use of solution NMR spectroscopy to determine the effect of organic solvents on chemical shift changes in bases on addition of acids is reported. This information can be useful in the evaluation of solvents and counterion selection
R S K Vijayan et al.
Journal of molecular graphics & modelling, 27(3), 286-298 (2008-06-21)
Given the heterogeneity of GABA(A) receptor, the pharmacological significance of identifying subtype selective modulators is increasingly being recognized. Thus, drugs selective for GABA(A) alpha(3) receptors are expected to display fewer side effects than the drugs presently in clinical use. Hence
Kebin Li et al.
Analytical chemistry, 80(13), 4945-4950 (2008-05-30)
Arrays of Au nanowells (NWs) were fabricated by electron-beam lithography (EBL) and characterized by surface plasmon resonance (SPR) and surface-enhanced Raman scattering (SERS). It is revealed that these Au NW arrays exhibit multiple SP resonances that can be tuned by
Brad Herberich et al.
Journal of medicinal chemistry, 51(20), 6271-6279 (2008-09-27)
Investigations into the structure-activity relationships (SAR) of a series of phthalazine-based inhibitors of p38 are described. These efforts originated from quinazoline 1 and through rational design led to the development of a series of orally bioavailable, potent, and selective inhibitors.
Jin Sung Kim et al.
Bioorganic & medicinal chemistry, 16(8), 4545-4550 (2008-03-07)
Studies on antitumor heterocyclic quinones containing nitrogens revealed that the number and position of nitrogens on the heterocyclic ring have significance on cytotoxicity of quinones. In our continuous effort to find more cytotoxic quinone compounds, we designed triazolophthalazine analogues in
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