2-Acetyl-4-chloro-6-nitrophenol
Names
[ CAS No. ]:
84942-40-5
[ Name ]:
2-Acetyl-4-chloro-6-nitrophenol
[Synonym ]:
1-(5-Chloro-2-hydroxy-3-nitrophenyl)ethanone
MFCD01631131
2-HYDROXY-3-NITROACETOPHENONE
5'-CHLORO-2'-HYDROXY-3'-NITROACETOPHE
1-acetyl-5-chloro-2-hydroxy-3-nitrobenzene
Ethanone, 1-(5-chloro-2-hydroxy-3-nitrophenyl)-
2-Acetyl-6-nitro-4-chloro phenol
2'-HYDROXY-3'-NITRO-5'-CHLORO ACETOPHENONE
1-(5-CHLORO-2-HYDROXY-3-NITRO-PHENYL)ETHANONE
5-Chloro-2-Hydroxy-3-Nitroacetophenone
5-CHLORO -3-NITRO-2-HYDROXY ACETOPHENONE
2-ACETYL-6-NITRO-4-CHLOROPHENOL
5'-Chloro-2'-hydroxy-3'-nitroacetophenone
2-Acetyl-4-chloro-6-nitrophenol
Chemical & Physical Properties
[ Density]:
1.5±0.1 g/cm3
[ Boiling Point ]:
260.7±40.0 °C at 760 mmHg
[ Melting Point ]:
132-135ºC
[ Molecular Formula ]:
C8H6ClNO4
[ Molecular Weight ]:
215.590
[ Flash Point ]:
111.5±27.3 °C
[ Exact Mass ]:
214.998535
[ PSA ]:
83.12000
[ LogP ]:
3.57
[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C
[ Index of Refraction ]:
1.609
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:Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S36
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2914700090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2914700090
[ Summary ]:
HS: 2914700090 halogenated, sulphonated, nitrated or nitrosated derivatives of ketones and quinones, whether or not with other oxygen function Tax rebate rate:9.0% Supervision conditions:none VAT:17.0% MFN tariff:5.5% General tariff:30.0%
Articles
Acta Crystallogr. Sect. E Struct. Rep. Online 70(Pt 5) , o547, (2014)
In the title compound, C10H4ClNO5, the non-H atoms of the 6-chloro-chromone unit are coplanar (r.m.s. deviation = 0.017 Å) with the largest deviation from the mean plane [0.031 (2) Å] being found for ...
Phase transition and intramolecular hydrogen bonding in nitro derivatives of ortho-hydroxy acetophenones Filarowski, A., et al.J. Mol. Struct. 785(1) , 7-13, (2006)