CAS 149719-06-2
:3-(piperidin-1-yl)propyl 4-amino-5-chloro-2-methoxybenzoate hydrochloride (1:1)
Description:
3-(Piperidin-1-yl)propyl 4-amino-5-chloro-2-methoxybenzoate hydrochloride is a chemical compound characterized by its complex structure, which includes a piperidine ring and a benzoate moiety. This substance is typically classified as a pharmaceutical intermediate or active ingredient, often utilized in medicinal chemistry for its potential therapeutic properties. The presence of the piperidine group suggests it may exhibit psychoactive or analgesic effects, while the chloro and methoxy substituents on the aromatic ring can influence its biological activity and solubility. As a hydrochloride salt, it is likely to be more soluble in water compared to its free base form, enhancing its bioavailability. The compound's molecular interactions, stability, and reactivity are influenced by its functional groups, making it a subject of interest in drug development. Safety and handling precautions are essential due to its chemical nature, and it should be stored in a controlled environment to maintain its integrity.
Formula:C16H24Cl2N2O3
InChI:InChI=1/C16H23ClN2O3.ClH/c1-21-15-11-14(18)13(17)10-12(15)16(20)22-9-5-8-19-6-3-2-4-7-19;/h10-11H,2-9,18H2,1H3;1H
SMILES:COc1cc(c(cc1C(=O)OCCCN1CCCCC1)Cl)N.Cl
Synonyms:- 3-(Piperidine-1-Yl)Propyl 4-Amino-5-Chloro-2-Methoxybenzoate Hydrochloride
- Benzoic acid, 4-amino-5-chloro-2-methoxy-, 3-(1-piperidinyl)propyl ester, hydrochloride (1:1)
- Benzoic acid, 4-amino-5-chloro-2-methoxy-, 3-(piperidine-1-yl)propyl ester, hydrochloride
- 3-(Piperidin-1-yl)propyl 4-amino-5-chloro-2-methoxybenzoate hydrochloride (1:1)
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Found 4 products.
3-(Piperidin-1-yl)propyl 4-amino-5-chloro-2-methoxybenzoate hydrochloride
CAS:<p>3-(Piperidin-1-yl)propyl 4-amino-5-chloro-2-methoxybenzoate hydrochloride</p>Purity:98%Molecular weight:363.29g/molRS 23597-190 Hydrochloride
CAS:<p>RS 23597-190 Hydrochloride is a selective serotonin receptor antagonist, which is a synthetic compound. It is derived from a targeted synthesis process designed to interact explicitly with serotonin receptors in the central nervous system. The mode of action involves binding to serotonin receptors, specifically targeting serotonin subtype receptors, thereby inhibiting their activity. This modulation can impact neurotransmission, influencing serotonin pathways which are foundational to various physiological and psychological processes.</p>Formula:C16H23ClN2O3·HClPurity:Min. 95%Molecular weight:326.82 g/molRS 23597-190 hydrochloride
CAS:<p>RS 23597-190 hydrochloride is a 5-HT4 receptor antagonist.</p>Formula:C16H24Cl2N2O3Purity:98%Color and Shape:SolidMolecular weight:363.28




