"Arylhydrazine" Example Sentences
1. Arylhydrazine is commonly used in the synthesis of azo dyes.
2. The reaction of arylhydrazine with aldehydes results in hydrazones.
3. The toxicity of arylhydrazines is a major concern in the chemical industry.
4. The substitution of arylhydrazines with halogens is an important reaction in organic chemistry.
5. The development of new methods for the preparation of arylhydrazines is an active area of research.
6. The use of arylhydrazines as reducing agents in organic synthesis has been well-documented.
7. The reactivity of arylhydrazine depends on the nature of the aryl group.
8. Arylhydrazines can undergo oxidative coupling to form azo compounds.
9. The aromatic ring of arylhydrazines makes them highly reactive towards electrophiles.
10. The synthesis of arylhydrazines can be accomplished through several methods, including diazotization and reduction.
11. The reaction of arylhydrazine with nitrous acid yields diazonium salts.
12. The use of arylhydrazines as intermediates in the synthesis of pharmaceuticals is an important application of this compound.
13. The substitution of arylhydrazine with methyl groups results in the formation of N,N-dimethylhydrazine.
14. The use of arylhydrazines in the preparation of azines is a convenient method for the synthesis of heterocycles.
15. The reactivity of arylhydrazines towards nucleophiles can be controlled through the substitution pattern of the aryl group.
16. The use of arylhydrazines in the preparation of nitrogen-containing heterocyclic compounds is an active area of research.
17. Arylhydrazines can be converted to corresponding hydrazones by reaction with ketones.
18. The reaction of arylhydrazine with carbonyl compounds can be used to prepare α-hydrazino ketones.
19. The aromaticity of the aryl group in arylhydrazines plays a crucial role in their reactivity.
20. The N–N bond in arylhydrazines is weaker than the N–N bond in hydrazine due to the influence of the aryl group.
21. The reaction of arylhydrazine with aromatic aldehydes results in the formation of bis(arylhydrazones).
22. The use of arylhydrazines in the synthesis of azoles is an important application of this compound.
23. The reduction of arylhydrazines by catalytic hydrogenation results in the formation of corresponding hydrazines.
24. Arylhydrazines can be used as precursors for the preparation of primary amines.
25. The use of arylhydrazines in the preparation of 1,2,4-triazoles is an important application of this compound.
26. The reaction of arylhydrazine with carboxylic acids results in the formation of corresponding hydrazides.
27. The reactivity of arylhydrazines towards electrophiles can be exploited in the synthesis of novel polyaromatic compounds.
28. The use of arylhydrazines in the synthesis of heterocyclic compounds with antimicrobial activity has been reported.
29. The N–N bond in arylhydrazines is susceptible to cleavage by light or heat.
30. The conversion of arylhydrazines to corresponding nitro compounds can be achieved through reaction with nitric acid.
Common Phases
1.
Arylhydrazine is used as a reactant in many organic synthesis reactions;
2.
Arylhydrazine derivatives have potential applications as anticancer agents;
3.
Arylhydrazine compounds are extensively studied for their biological activities;
4. The synthesis of
arylhydrazines involves multi-step procedures and careful reaction conditions;
5. The use of
arylhydrazines in medicinal chemistry has recently gained attention due to their diverse pharmacological activities;
6.
Arylhydrazine derivatives have shown promising results in the treatment of various neurodegenerative disorders;
7. The development of novel
arylhydrazine-based compounds is an active area of research in organic chemistry;
8. The aromatic ring of
arylhydrazines plays a crucial role in determining their physical and chemical properties;
9. Some
arylhydrazines have been reported to exhibit insecticidal and fungicidal activities;
10.
Arylhydrazines are commonly used as starting materials for the preparation of diverse chemical compounds.