Details
Quality products?make an important contribution to long-term revenue and profitability. Bulk supply high purity 4-Nitrobenzaldoxime 1129-37-9, Paid sample available
1.What is the 4-Nitrobenzaldoxime ?
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4-nitro-benzaldehyde-(O -[1]naphthylcarbamoyl-(E )-oxime ); α-naphthylcarbamic acid-derivative of 4-nitro-α-benzaldoxime
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furan-2,3,5(4H)-trione pyridine (1:1)
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1129-37-9,174848-02-3,20707-69-1
4-nitrobenzaldehyde oxime
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607-56-7
1,3-dinaphthalen-1-ylurea
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134-32-7
1-amino-naphthalene
| Conditions | Yield |
|---|---|
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|
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555-16-8
4-nitrobenzaldehdye
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619-72-7
4-nitrobenzonitrile
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1129-37-9,174848-02-3,20707-69-1
4-nitrobenzaldehyde oxime
| Conditions | Yield |
|---|---|
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With
hydroxylamine hydrochloride; titanium(IV) oxide;
for 0.0833333h;
Microwave irradiation;
Neat (no solvent);
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With
ammonium hydroxide; dihydrogen peroxide;
In
water;
at 20 ℃;
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With
hydroxylamine hydrochloride;
In
acetonitrile;
at 70 - 110 ℃;
chemoselective reaction;
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2.What is the CAS number for 4-Nitrobenzaldoxime ?
The CAS number of 4-Nitrobenzaldoxime is 1129-37-9.
More information of 4-Nitrobenzaldoxime 1129-37-9 are:
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CAS?Number |
1129-37-9 |
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Density |
1.33 g/cm3 |
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Melting Point |
126-130 °C(lit.) |
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Boiling Point |
304.2 °C at 760 mmHg |
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Flash Point |
137.8 °C |
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Vapor Pressure |
0.00039mmHg at 25°C |
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Refractive Index |
1.5880 (estimate) |
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HS CODE |
29280000 |
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PSA |
78.41000 |
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LogP |
1.92610 |
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Pka |
9.97±0.10(Predicted) |
3.What are another words for 4-Nitrobenzaldoxime ?
Synonyms?for?4-Nitrobenzaldoxime 1129-37-9:Benzaldehyde,p-nitro-, oxime (6CI,7CI,8CI);(4-Nitrobenzylidene)hydroxylamine;4-Nitrobenzaldehyde oxime;4-Nitrobenzaldoxime;NSC 68355;p-Nitrobenzaldehydeoxime;p-Nitrobenzaldoxime;
4.What is the molecular formula of 4-Nitrobenzaldoxime?
The chemical formula of ?4-Nitrobenzaldoxime is?C7H6N2O3 which containing 7 Carbon atoms,6 Hydrogen atoms,2 Nitrogen atoms and 3 Oxygen atoms,and the molecular weight of??4-Nitrobenzaldoxime?is 166.136.
5.What is 4-Nitrobenzaldoxime (1129-37-9) used for?
4-Nitrobenzaldoxime is a versatile intermediate that can undergo various transformations, including rearrangement to E- or Z-oxime structures depending on reaction conditions and steric factors. It reacts with hydroxylaminothiazolidine-2-thiones to form stable nitrones, which may further hydrolyze under acid-catalysis to yield 4-hydroxy derivatives and E-4-nitrobenzaldoxime. 4-Nitrobenzaldoxime's reactivity highlights its utility in synthetic chemistry, particularly in the formation of nitrones and oximes with potential applications in organic synthesis and medicinal chemistry.
InChI:InChI=1/C7H6N2O3/c10-8-5-6-1-3-7(4-2-6)9(11)12/h1-5,10H/b8-5-
Relevant articles related to 4-Nitrobenzaldoxime:
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Article |
Source |
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Efficient preparation of aldoximes from arylaldehydes, ethylenediamine and Oxone in water |
Xia, Jing-Jing,Wang, Guan-Wu , p. 231 - 236 (2007) |
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A rapid and convenient method for the synthesis of aldoximes under microwave irradiation using in situ generated ionic liquids |
Hajipour,Rafiee,Ruoho , p. 114 - 118 (2010) |
6.Buy 4-Nitrobenzaldoxime with the best price .
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