1450-76-6
- Product Name：2-Hydroxy-5-nitroacetophenone
- Molecular Formula：C8H7NO4
- Purity：99%
- Molecular Weight：181.148
Product Details;
CasNo： 1450-76-6
Molecular Formula： C8H7NO4
factory and supplier 1450-76-6 2-Hydroxy-5-nitroacetophenone in stock
- Molecular Formula:C8H7NO4
- Molecular Weight:181.148
- Vapor Pressure:0.00163mmHg at 25°C
- Melting Point:100-104 °C(lit.)
- Boiling Point:285.5 °C at 760 mmHg
- PKA:7.27±0.22(Predicted)
- Flash Point:126 °C
- PSA：83.12000
- Density:1.38 g/cm3
- LogP:2.02620
2'-HYDROXY-5'-NITROACETOPHENONE(Cas 1450-76-6) Usage
InChI:InChI=1/C8H7NO4/c1-5(10)7-4-6(9(12)13)2-3-8(7)11/h2-4,11H,1H3/p-1
1450-76-6 Relevant articles
A new and improved process for celiprolol hydrochloride
Joshi, Ramesh A.,Gurjar, Mukund K.,Tripathy, Narendra K.,Chorghade, Mukund S.
, p. 176 - 178 (2001)
Celiprolol hydrochloride, a β-blocker dr...
Design, synthesis and biological evaluation of novel benzopyran sulfonamide derivatives as 5-HT6 receptor ligands
Nirogi, Ramakrishna V. S.,Badange, Rajeshkumar,Reballi, Veena,Khagga, Mukkanti
, p. 2117 - 2124 (2015)
On the basis of a known pharmacophore mo...
Sigma Complexes in the Pyrimidine Series. 6. Reaction of 5-Nitro-2-methoxy- and 5-Nitro-4,6-dimethoxypyrimidines with the Acetylacetone Carbanion
Remennikov, G. Ya.,Kisilenko, A. A.,Cherkasov, V. M.
, p. 1109 - 1112 (1983)
Depending on the reaction conditions, th...
Raf kinase inhibitor based on chromone structure, and preparation method and uses thereof
-
Paragraph 0160; 0161; 0162, (2016/10/07)
The invention relates to the technical f...
A kind of two-thiazoline ketone compounds and pharmaceutical compositions thereof and use thereof (by machine translation)
-
Paragraph 0091; 0092, (2017/01/17)
The invention provides general formula (...
8-nitro-2-four azolyl-4- carbonyl benzene benzopyran synthetic method
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Paragraph 0033; 0034; 0035, (2017/02/24)
The invention relates to a synthesis met...
1450-76-6 Process route
-
-
123-54-6,81235-32-7
acetylacetone
-
-
14080-32-1
5-nitropyrimidine
-
-
21203-68-9
2-methyl-5-nitropyridine
-
-
1450-76-6
1-(2-hydroxy-5-nitrophenyl)ethanone
-
-
16475-85-7
1,1'-(4-hydroxy-6-methyl-1,3-phenylene)diethanone
| Conditions | Yield |
|---|---|
|
With
potassium hydroxide;
In
methanol;
for 5h;
Heating;
|
3.5% 3% 4% |
|
With
potassium hydroxide;
In
methanol;
for 5h;
Heating;
|
3.5% 4% 3% |
|
With
potassium hydroxide;
In
methanol;
for 5h;
Heating;
|
3% 4% 3.5% |
-
-
100-02-7,78813-13-5,89830-32-0
4-nitro-phenol
-
-
75-36-5
acetyl chloride
-
-
1450-76-6
1-(2-hydroxy-5-nitrophenyl)ethanone
| Conditions | Yield |
|---|---|
|
With
aluminum (III) chloride;
In
1,1-dichloroethane;
at 50 ℃;
for 2h;
|
78% |
|
With
aluminum (III) chloride;
In
1,2-dichloro-ethane;
at 50 ℃;
for 2h;
|
78% |
|
With
aluminium trichloride; nitrobenzene;
at 120 - 130 ℃;
|
1450-76-6 Upstream products
-
51484-05-0
6-nitro-chromen-4-one
-
100-02-7
4-nitro-phenol
-
108-24-7
acetic anhydride
-
118-93-4
o-hydroxyacetophenone
1450-76-6 Downstream products
-
23398-90-5
2'-hydroxy-3,4-methylenedioxy-5'-nitro-trans-chalcone
-
3316-09-4
1,2-dihydroxy-4-nitrobenzene
-
35234-45-8
(E)-1-(2-hydroxy-5-nitrophenyl)-3-phenylprop-2-en-1-one
-
1776-26-7
2'-hydroxy-4-methoxy-5'-nitro-trans-chalcone
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