ChemAbout
© 2026 ChemAbout
Insights|Privacy Policy|Terms of Service|[email protected]
Home/Compounds/Research Reagent/(S)-3-(4-Bromophenyl)piperidine
C11H14BrN
240.14 g/mol
Research Reagent

(S)-3-(4-Bromophenyl)piperidine

CAS1335523-82-4
Category
Research Reagent
Compound Class
Amine
Primary Use
Research Compound

(S)-3-(4-Bromophenyl)piperidine is a chiral research compound featuring a piperidine ring substituted with a bromophenyl group. It is structurally related to cyclized phenethylamine derivatives and is used primarily in laboratory and developmental research.

research compound for chemical and biological studieslaboratory reagent in synthetic chemistry

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.

Sourcing or supplying this compound?

List your inventory or post a purchase request

CAS 1335523-82-4

List This Product
Sign in to publish supply information
Request This Product
Submit a request without registering

Related Compounds

StrongSame Parent

(S)-3-(4-bromophenyl)piperidine hydrochloride

CAS2141967-71-5

pharmaceutical intermediate

ReferenceSame Category

3,5-dimethyl-d6-phenol

CAS133604-75-8

research compound

ReferenceSame Category

4-(Trimethylsilyl)morpholine

CAS13368-42-8

research compound

ReferenceSame Category

Butyltriphenylphosphonium chloride

CAS13371-17-0

research compound

ReferenceSame Category

N-(trifluoromethanesulfonyloxy)-5-norbornene-2,3-dicarboximide

CAS133710-62-0

research compound

Referencestereoisomer of

3-(4-Bromophenyl)piperidine

CAS769944-72-1

pharmaceutical intermediate

Referencesame scaffold

(S)-3-Phenylpiperidine

CAS59349-71-2

pharmaceutical intermediate

Referencesame scaffold

Tert-Butyl (3s)-3-(4-bromophenyl)-piperidine-1-carboxylate

CAS1476776-55-2

pharmaceutical intermediate

Identifiers
IUPAC Name

(3S)-3-(4-bromophenyl)piperidine

InChIKey

SZTZMTODFHPUHI-SNVBAGLBSA-N

SMILES

C1C[C@H](CNC1)C2=CC=C(C=C2)Br

Synonyms (2)

—