CAS 61886-17-7
:4-Phenyl-1-(phenylmethyl)-4-piperidinecarboxylic acid
Description:
4-Phenyl-1-(phenylmethyl)-4-piperidinecarboxylic acid, with the CAS number 61886-17-7, is a chemical compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. This compound features a phenyl group and a benzyl group attached to the piperidine, contributing to its lipophilicity and potential biological activity. It is typically a white to off-white solid at room temperature and is soluble in organic solvents, though its solubility in water may be limited. The presence of the carboxylic acid functional group indicates that it can participate in acid-base reactions and may form salts with bases. This compound is of interest in medicinal chemistry, particularly for its potential pharmacological properties, which may include analgesic or anti-inflammatory effects. As with many piperidine derivatives, it may interact with various biological targets, making it a subject of research in drug development. Proper handling and safety measures should be observed due to its chemical nature.
Formula:C19H21NO2
InChI:InChI=1/C19H21NO2/c21-18(22)19(17-9-5-2-6-10-17)11-13-20(14-12-19)15-16-7-3-1-4-8-16/h1-10H,11-15H2,(H,21,22)
InChI key:InChIKey=RYTBNRKHWAWLPQ-UHFFFAOYSA-N
SMILES:C(O)(=O)C1(CCN(CC2=CC=CC=C2)CC1)C3=CC=CC=C3
Synonyms:- 4-Phenyl-1-phenylmethylpiperidine-4-carboxylic acid
- Isonipecotic acid, 1-benzyl-4-phenyl-
- 4-Piperidinecarboxylic acid, 4-phenyl-1-(phenylmethyl)-
- 1-Benzyl-4-phenyl-4-piperidinecarboxylic acid
- 4-Phenyl-1-(phenylmethyl)-4-piperidinecarboxylic acid
- 1-Benzyl-4-phenylpiperidine-4-carboxylic acid
- 1-Benzyl-4-phenylpiperidine-4-carbo
- Oxytocin Impurity 1 Trifluoroacetate
- 1-benzyl-4-phenylpiperidine-4-carboxylic acid(SALTDATA: 0.6H2O)
- Pethidine Hydrochloride EP Impurity F
- Pethidine Hydrochloride Impurity F
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Found 2 products.
1-Benzyl-4-phenylpiperidine-4-carboxylic acid
CAS:Controlled Product1-Benzyl-4-phenylpiperidine-4-carboxylic acid (1BPPC) is a soluble guanylate cyclase activator that is used as a research tool. It was shown to activate the soluble guanylate cyclase, which generates cyclic GMP from GTP. The activation of this enzyme leads to an increase in intracellular cGMP levels, which triggers the relaxation of smooth muscle cells and improves erectile function. 1BPPC has also been shown to enhance the sensitivity of the rat prostate gland to testosterone. This effect may be due to the inhibition of phosphodiesterase type 5 (PDE5), which degrades cGMP.Formula:C18H21NO2Purity:Min. 95%Molecular weight:283.36 g/mol

