- CAS
- Purity
- 110035-28-4
- 99%
Location:Home > Pharmaceutical
Quality products?make an important contribution to long-term revenue and profitability. Buy Quality Pyrazole-1,3-dimethyl-5-phenoxy-4-carboxaldehyde oxime 110035-28-4 In Stock with Immediately Delivery
Used in Medicinal Chemistry:
Pyrazole-1,3-dimethyl-5-phenoxy-4-carboxaldehyde oxime is used as a building block in the development of pharmaceuticals for its potential to contribute to the creation of new drugs with unique therapeutic properties.
Used in Agrochemical Development:
Pyrazole-1,3-dimethyl-5-phenoxy-4-carboxaldehyde oxime is also utilized in the synthesis of agrochemicals, where it can serve as a key intermediate for the development of novel pesticides or other agricultural products.
Used in Organic Synthesis:
Pyrazole-1,3-dimethyl-5-phenoxy-4-carboxaldehyde oxime is used as a versatile intermediate in organic synthesis, allowing for the creation of a wide range of heterocyclic compounds and organic intermediates that can be applied across various chemical industries.
Used in Research and Development:
In the field of research and development, Pyrazole-1,3-dimethyl-5-phenoxy-4-carboxaldehyde oxime is employed as a valuable compound for exploring new chemical reactions and mechanisms, potentially leading to innovative applications in various industries.
1,3-dimethyl-5-phenoxypyrazole-4-carbaldehyde
1,3-dimethyl-5-phenoxy-1H-pyrazole-4-carbaldehyde oxime
| Conditions | Yield |
|---|---|
|
With
hydroxylamine hydrochloride; potassium hydroxide;
In
methanol;
|
|
|
With
hydroxylamine hydrochloride; potassium hydroxide;
Reflux;
|
|
|
With
hydroxylamine hydrochloride; potassium hydroxide;
Reflux;
|
|
|
With
hydroxylamine hydrochloride; sodium hydroxide;
In
ethanol; water;
at 20 - 30 ℃;
for 0.5h;
|
5-chloro-4-formyl-1,3-dimethylpyrazole
1,3-dimethyl-5-phenoxy-1H-pyrazole-4-carbaldehyde oxime
| Conditions | Yield |
|---|---|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / N,N-dimethyl-formamide / 40 - 110 °C
2: potassium hydroxide; hydroxylamine hydrochloride / methanol
With
hydroxylamine hydrochloride; potassium hydroxide;
In
methanol; N,N-dimethyl-formamide;
|
|
|
Multi-step reaction
with
2
steps
1.1: sodium hydroxide / ethanol / Reflux
1.2: 105 °C
2.1: hydroxylamine hydrochloride; potassium hydroxide / Reflux
With
hydroxylamine hydrochloride; potassium hydroxide; sodium hydroxide;
In
ethanol;
|
|
|
Multi-step reaction
with
2
steps
1.1: potassium hydroxide / 2 h / 45 °C
1.2: 110 °C
2.1: potassium hydroxide; hydroxylamine hydrochloride / Reflux
With
hydroxylamine hydrochloride; potassium hydroxide;
|
|
|
Multi-step reaction
with
2
steps
1.1: potassium hydroxide / N,N-dimethyl-formamide / 6 h / 40 °C
1.2: 100 °C
2.1: hydroxylamine hydrochloride; sodium hydroxide / ethanol; water / 0.5 h / 20 - 30 °C
With
hydroxylamine hydrochloride; potassium hydroxide; sodium hydroxide;
In
ethanol; water; N,N-dimethyl-formamide;
|
The CAS number of Pyrazole-1,3-dimethyl-5-phenoxy-4-carboxaldehyde oxime is 110035-28-4.
More information of Pyrazole-1,3-dimethyl-5-phenoxy-4-carboxaldehyde oxime 110035-28-4 are:
|
CAS?Number |
110035-28-4 |
|
Density |
1.21 g/cm3 |
|
Melting Point |
133-134 °C |
|
Boiling Point |
359.4 °C at 760 mmHg |
|
Flash Point |
171.2 °C |
|
HS CODE |
2933199090 |
|
PSA |
57.42000 |
|
LogP |
0.91650 |
|
Pka |
10.45±0.10(Predicted) |
Synonyms?for?Pyrazole-1,3-dimethyl-5-phenoxy-4-carboxaldehyde oxime 110035-28-4:1,3-Dimethyl-5-phenoxy-1H-pyrazole-4-carbaldehydeoxime;1,3-Dimethyl-5-phenoxy-1H-pyrazole-4-carboxaldehyde oxime;
The chemical formula of ?Pyrazole-1,3-dimethyl-5-phenoxy-4-carboxaldehyde oxime is?C12H13N3O2 which containing 12 Carbon atoms,13 Hydrogen atoms,3 Nitrogen atoms and 2 Oxygen atoms,and the molecular weight of??Pyrazole-1,3-dimethyl-5-phenoxy-4-carboxaldehyde oxime?is 231.254.
Pyrazole-1,3-dimethyl-5-phenoxy-4-carboxaldehyde oxime is a versatile chemical compound characterized by a pyrazole ring with a dimethyl substituent at the 1 and 3 positions, a phenoxy group at the 5 position, and a carboxaldehyde oxime at the 4 position. It is widely recognized for its potential applications in medicinal chemistry, including the development of pharmaceuticals and agrochemicals, as well as in the synthesis of heterocyclic compounds and organic intermediates due to its diverse reactivity.
Relevant articles related to Pyrazole-1,3-dimethyl-5-phenoxy-4-carboxaldehyde oxime:
|
Article |
Source |
|
Synthesis and bioactivities of novel pyrazole oxime derivatives containing a 5-trifluoromethylpyridyl moiety |
Dai, Hong,Chen, Jia,Li, Hong,Dai, Baojiang,He, Haibing,Fang, Yuan,Shi, Yujun , (2016/04/20) |
|
The thiazoylmethoxy modification on pyrazole oximes: Synthesis and insecticidal biological evaluation beyond acaricidal activity |
Dai, Hong,Xiao, Yan-Shuang,Li, Zhong,Xu, Xiao-Yong,Qian, Xu-Hong , p. 1014 - 1016 (2014/08/18) |
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