2-((3-Trifluoromethyl)phenyl)histamine D, identified by its CAS number 162049-83-4, is a chemical compound that belongs to the class of histamine derivatives. This substance features a histamine backbone modified with a 3-trifluoromethylphenyl group, which enhances its pharmacological properties. The trifluoromethyl group is known for its electron-withdrawing effects, which can influence the compound's reactivity and interaction with biological targets. Typically, compounds like this are studied for their potential roles in modulating histamine receptors, which are crucial in various physiological processes, including allergic responses and neurotransmission. The presence of fluorine atoms often contributes to increased lipophilicity and metabolic stability, making such compounds of interest in medicinal chemistry. Additionally, the specific structural modifications can lead to variations in potency and selectivity towards different histamine receptor subtypes, which is essential for developing targeted therapeutic agents. Overall, 2-((3-trifluoromethyl)phenyl)histamine D represents a significant area of research in the context of drug development and receptor pharmacology.

2-((3-TRIFLUOROMETHYL)PHENYL)HISTAMINE D

162049-83-4: 2-((3-Trifluoromethyl)phenyl)histamine D, identified by its CAS number 162049-83-4, is a chemical compound that belongs to the class of histamine derivatives. This substance features a histamine backbone modified with a 3-trifluoromethylphenyl group, which enhances its pharmacological properties. The trifluoromethyl group is known for its electron-withdrawing effects, which can influence the compound's reactivity and interaction with biological targets. Typically, compounds like this are studied for their potential roles in modulating histamine receptors, which are crucial in various physiological processes, including allergic responses and neurotransmission. The presence of fluorine atoms often contributes to increased lipophilicity and metabolic stability, making such compounds of interest in medicinal chemistry. Additionally, the specific structural modifications can lead to variations in potency and selectivity towards different histamine receptor subtypes, which is essential for developing targeted therapeutic agents. Overall, 2-((3-trifluoromethyl)phenyl)histamine D represents a significant area of research in the context of drug development and receptor pharmacology.

CAS 162049-83-4

2-((3-TRIFLUOROMETHYL)PHENYL)HISTAMINE D

1H-Imidazole-4-ethanamine, 2-[3-(trifluoromethyl)phenyl]-, (2Z)-2-butenedioate (1:2) (9CI)

Ref: IN-DA001SOS

2-((3-Trifluoromethyl)phenyl)histamine dimaleate

Ref: 7W-GK1278

T 4951

Ref: TR-T002700