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3-Chloro-6-phenylpyridazine

Names

[ CAS No. ]:
20375-65-9

[ Name ]:
3-Chloro-6-phenylpyridazine

[Synonym ]:
3-Chloro-6-phenylpyridazine
3-chloro-6-phenyl pyridazine
3-Chlor-6-phenyl-pyridazin
MFCD00075253
EINECS 243-772-6
6-chloro-3-phenylpyridazine
Pyridazine, 3-chloro-6-phenyl-
6-phenyl-3-chloropyridazine
2-chloro-6-phenylpyridazine
3-phenyl-6-chloropyridazine

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
375.0±22.0 °C at 760 mmHg

[ Melting Point ]:
159-161 °C(lit.)

[ Molecular Formula ]:
C10H7ClN2

[ Molecular Weight ]:
190.629

[ Flash Point ]:
212.4±7.9 °C

[ Exact Mass ]:
190.029770

[ PSA ]:
25.78000

[ LogP ]:
1.98

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.594

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2942000000

Synthetic Route

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Synthesis, antitubercular, antifungal and antibacterial activities of 6-substituted phenyl-2-(3'-substituted phenyl pyridazin-6'-yl)-2,3,4,5-tetrahydropyridazin-3-one.

Acta Pol. Pharm. 65(3) , 353-62, (2008)

A series of 6-substituted phenyl-2-(3'-substituted phenyl pyridazin-6'-yl)-2,3,4,5-tetrahydropyridazin-3-ones has been synthesized. An appropriate aromatic hydrocarbon reacts with succinic anhydride i...

Electrochemical carboxylation of some heteroaromatic compounds. Fuchs P, et al.

Acta Chem. Scand. B 35 , 185-92, (1981)

Selective and efficient fluorination of chlorodiazines under solvent-free phase transfer catalysis. Marque S, et al.

J. Fluor. Chem. 125(12) , 1847-51, (2004)


More Articles


Related Compounds

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