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Home/Compounds/Pharmaceutical Intermediate/4-[(4-Chlorophenyl)-2-pyridylmethoxy]piperidine p-nitrobenzoic acid salt
C24H24ClN3O5
469.9 g/mol
Pharmaceutical Intermediate

2-((4-Chlorophenyl)(piperidin-4-yloxy)methyl)pyridine 4-nitrobenzoate

CAS161558-45-8
Category
Pharmaceutical Intermediate
Compound Class
Amine
Primary Use
Pharmaceutical Intermediate

This compound is a salt formed from a piperidine-containing pyridine derivative and 4-nitrobenzoic acid. It is primarily used as an intermediate in pharmaceutical manufacturing.

pharmaceutical intermediate

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

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Related Compounds

StrongSame Parent

2-[(4-Chlorophenyl)(4-piperidinyloxy)methyl]pyridine

CAS122368-54-1

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ReferenceSame Category

(S)-(+)-N-(2,3-Epoxypropyl)phthalimide

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ReferenceSame Category

4-(4-Methylaminocarbonylphenyl)piperidine

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pharmaceutical intermediate

ReferenceSame Category

Spiro[9H-fluorene-9,4'-piperidine]-1'-carboxylic acid, 2,7-dibromo-, 1,1-dimethylethyl ester

CAS1616113-98-4

pharmaceutical intermediate

ReferenceSame Category

2,5-Methanopyrido[1′,2′:4,5]pyrazino[2,1-b][1,3]oxazepine-10-carboxamide, 2,3,4,5,7,9,13,13a-octahydro-8-methoxy-7,9-dioxo-N-[(2,4,6-trifluorophenyl)methyl]-, (2R,5S,13aR)-

CAS1616340-94-3

pharmaceutical intermediate

Referencestereoisomer of

(S)-2-[(4-Chlorophenyl)(4-piperidinyloxy)methyl]pyridine

CAS201594-84-5

research compound

Referencestereoisomer of

2-[(S)-(4-Chlorophenyl)(4-piperidinyloxy)methyl]pyridine (2R,3R)-2,3-Dihydroxybutanedioate

CAS210095-58-2

pharmaceutical intermediate

Referencestereoisomer of

(S)-2-((4-Chlorophenyl)(piperidin-4-yloxy)methyl)pyridine (S)-2-acetamido-3-phenylpropanoate

CAS210095-66-2

research compound

Identifiers
IUPAC Name

2-[(4-chlorophenyl)-piperidin-4-yloxymethyl]pyridine;4-nitrobenzoic acid

InChIKey

UQSUJCNJGVBZCU-UHFFFAOYSA-N

SMILES

C1CNCCC1OC(C2=CC=C(C=C2)Cl)C3=CC=CC=N3.C1=CC(=CC=C1C(=O)O)[N+](=O)[O-]

Synonyms (7)

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