CAS 76811-98-8
:2-[4-[4-[4-(Hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl]phenyl]-2,2-dimethylacetic acid
Description:
2-[4-[4-[4-(Hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl]phenyl]-2,2-dimethylacetic acid, with CAS number 76811-98-8, is a complex organic compound characterized by its multi-functional structure. It features a piperidine ring, which contributes to its potential biological activity, and a hydroxydiphenylmethyl group that may enhance its interaction with biological targets. The presence of a dimethylacetic acid moiety suggests that it may exhibit acidic properties, which can influence its solubility and reactivity in various environments. This compound is likely to be lipophilic due to its aromatic and aliphatic components, which may affect its pharmacokinetics if used in medicinal chemistry. Additionally, the presence of multiple functional groups indicates potential for hydrogen bonding and other intermolecular interactions, which could be relevant in drug design and development. Overall, this compound's unique structure may confer specific biological activities, making it of interest in pharmaceutical research.
Formula:C32H37NO4
InChI:InChI=1S/C32H37NO4/c1-31(2,30(35)36)25-17-15-24(16-18-25)29(34)14-9-21-33-22-19-28(20-23-33)32(37,26-10-5-3-6-11-26)27-12-7-4-8-13-27/h3-8,10-13,15-18,28,37H,9,14,19-23H2,1-2H3,(H,35,36)
InChI key:InChIKey=NGAKDIWPTMPPFP-UHFFFAOYSA-N
SMILES:C(O)(C1CCN(CCCC(=O)C2=CC=C(C(C(O)=O)(C)C)C=C2)CC1)(C3=CC=CC=C3)C4=CC=CC=C4
Synonyms:- 2-(4-(4-(4-(Hydroxydiphenylmethyl)piperidin-1-yl)butanoyl)phenyl)-2-methylpropanoic acid
- 2-[4-[4-[4-(Hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl]phenyl]-2,2-dimethylacetic acid
- 4-[1-Oxo-4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]butyl]-α,α-dimethylbenzeneacetic acid
- 4-[4-[4-(Hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl]-α,α-dimethylbenzeneacetic acid
- 4-[4-[4-(Hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl]-α,α-dimethylphenylacetic acid
- Benzeneacetic acid, 4-[4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl]-α,α-dimethyl-
- Fexofenadinone
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Found 10 products.
Fexofenadine Related Compound A (2-(4-{4-[4-(Hydroxydiphenylmethyl)piperidin-1-yl]butanoyl}phenyl)-2-methylpropanoic acid)
CAS:Compounds containing an unfused pyridine ring in the structure, nesoiFormula:C32H37NO4Color and Shape:White PowderMolecular weight:499.27226Fexofenadine EP Impurity A (Fexofenadine USP Related Compound A)
CAS:Formula:C32H37NO4Color and Shape:White To Off-White SolidMolecular weight:499.652-(4-(4-(4-(Hydroxydiphenylmethyl)piperidin-1-yl)butanoyl)phenyl)-2-methylpropanoic acid (Fexofenadine Impurity)
CAS:2-(4-(4-(4-(Hydroxydiphenylmethyl)piperidin-1-yl)butanoyl)phenyl)-2-methylpropanoic acid (Fexofenadine Impurity)Purity:98%2-[4-[4-[4-(Hydroxydiphenylmethyl)piperidin-1-yl]butanoyl]phenyl]-2-methylpropanoic Acid (Ketofexofenadine)
CAS:Controlled ProductFormula:C32H37NO4Color and Shape:NeatMolecular weight:499.64Fexofenadinone Hydrochloride
CAS:Controlled Product<p>Applications The oxo analogue of Fexofenadine (F322470); H1-histamine receptor antagonist and an active metabolite of Terfenadine (T114500).<br>References Radhakrishna, T. et al.: J. Pharmac. Biomed. Anal., 29, 681 (2002); Chen, T.M. et al.: J. Pharmac. Biomed, Anal., 9, 929 (1991);<br></p>Formula:C32H37NO4•(HCl)xColor and Shape:NeatMolecular weight:499.64 + (36.46)Fexofenadinone
CAS:Controlled Product<p>Impurity Fexofenadine EP Impurity A<br>Stability Hygroscopic<br>Applications The oxo analogue of Fexofenadine (F322470); H1-histamine receptor antagonist and an active metabolite of Terfenadine (T114500).<br>References Radhakrishna, T. et al.: J. Pharmac. Biomed. Anal., 29, 681 (2002); Chen, T.M. et al.: J. Pharmac. Biomed, Anal., 9, 929 (1991);<br></p>Formula:C32H37NO4Color and Shape:NeatMolecular weight:499.644-((4-(4-Hydroxydiphenylmethyl)-1-piperidinyl)-1-oxobutyl)-a,a-dimethyl-phenylacetic acid
CAS:<p>Methyl ester of 4-((4-(4-hydroxydiphenylmethyl)-1-piperidinyl)-1-oxobutyl)-a,a-dimethylphenylacetic acid is a metabolite of lisinopril. It has been used to calibrate the flow rate of chromatographic methods by comparison with anhydrous standards. The methyl ester can be quantitatively converted to the sodium salt by photolysis in a diode laser. This method has been validated and found to be accurate for industrial process monitoring.</p>Formula:C32H37NO4Purity:Min. 95%Molecular weight:499.64 g/mol









