59808-52-5

Usage

Uses

Used in Pharmaceutical Industry:
2-Phenylpyrimidin-5-amine is used as a key intermediate in the synthesis of various pharmaceutical compounds for its potential to contribute to the development of new drugs and biologically active molecules.
Used in Organic Synthesis:
In the field of organic synthesis, 2-Phenylpyrimidin-5-amine is used as a building block to create complex molecules with specific properties and functions, contributing to the advancement of chemical research and the creation of novel materials.
Used in Medicinal Chemistry and Drug Discovery Research:
2-Phenylpyrimidin-5-amine is utilized in medicinal chemistry and drug discovery research as a subject of interest due to its potential biological activities and pharmacological effects, which may lead to the identification of new therapeutic agents.

InChI:InChI=1/C10H9N3/c11-9-6-12-10(13-7-9)8-4-2-1-3-5-8/h1-7H,11H2

Upstream product

• 68906-00-3 2-phenyl-5-nitropyrimidine 
• 1670-14-0 benzamidine monohydrochloride 

Downstream Products

• 144658-04-8 N-(2-phenylpyrimidin-5-yl)benzamidine 
• 1354652-65-5 N₁-methyl-N₁-(2-morpholinoethyl)-N₃-(2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)isophthalamide 
• 1354652-56-4 3-(3-((2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)-carbamoyl)benzylthio)benzoic acid 
• 1354652-82-6 2-(3-(bromomethyl)benzamido)-N-(2-phenylpyrimidin-5-yl)-5-(piperidin-1-yl)benzamide 
• 1354652-55-3 3-((3-((2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)carbamoyl)benzyl)thio)propanoic acid 
• 1354652-81-5 methyl 3-((3-((2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)carbamoyl)-benzyl)thio)propanoate 
• 1354652-80-4 2-amino-N-(2-phenylpyrimidin-5-yl)-5-(piperidin-1-yl)benzamide 
• 1354652-69-9 C₄₀H₄₆N₆O₈ 
• 1354653-07-8 C₄₄H₅₄N₆O₈ 
• 1354653-06-7 3-((2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)carbamoyl)benzoic acid 
• 1354653-05-6 methyl 3-((2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)carbamoyl)benzoate 
• 1230021-47-2 (2-phenyl-pyrimidin-5-yl)-carbamic acid phenyl ester 

Relevant academic research and scientific papers

1-azinyl-tetrazolinones

1-Azinyl-tetraozolinones of the following formulae (I) and (II): STR1 wherein R1 and R2 are independently represent alkyl, haloalkyl, cycloalkyl, alkenyl, haloalkenyl, alkynyl or optionally substituted phenyl, or R1 and R2, together with the nitrogen atom to which they are bonded, may form a 5- or 6-membered heterocyclic ring which may optionally contain a further heteroatom, and said heterocyclic ring may optionally be benzo-condensed and/or be substituted by one or more of C1-4 alkyl(s), and R3 is a 6-membered heterocyclic aromatic group consisting of carbon atoms and 2 or 3 nitrogen atoms, which may optionally be substituted by halogen, C1-4 alkyl, C1-4 alkoxy, C1-4 alkylthio, di(C1-4 alkyl)amino or phenyl. The compounds of the formula (I) exhibit an excellent herbicidal activity and the compounds of the formula (II) are useful as starting materials in the production of the compounds of the formula (I).

SYNTHESIS OF SCHIFF BASES OF 2-SUBSTITUTED 5-AMINOPYRIMIDINES AND THEIR MESOMORPHIC PROPERTIES

Schiff bases of 2-substituted 5-aminopyrimidines were synthetized, and their liquid-crystal and dielectric properties were investigated.It is shown that narrow ranges of the existence of meso phases and a greater (as compared with benzyllideneanilines) te