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Home/Compounds/Research Reagent/Rac-tert-butyl (3R,4S)-3-amino-4-fluoropiperidine-1-carboxylate
C10H19FN2O2
218.27 g/mol
Research ReagentDanger

Rac-tert-butyl (3R,4S)-3-amino-4-fluoropiperidine-1-carboxylate

CAS1290191-73-9EC968-900-4
Category
Research Reagent
Compound Class
Amine
Primary Use
Research Compound

This compound is a fluorinated piperidine derivative featuring an amino group and a tert-butoxycarbonyl (Boc) protecting group. It is primarily used as a research reagent in organic synthesis and medicinal chemistry studies.

Building block in pharmaceutical researchIntermediate for the synthesis of biologically active molecules

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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CAS 1290191-73-9

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Referencestereoisomer of

TERT-BUTYL 3-AMINO-4-FLUOROPIPERIDINE-1-CARBOXYLATE

CAS1334414-00-4

pharmaceutical intermediate

Referencestereoisomer of

Tert-butyl (3R,4S)-3-amino-4-fluoropiperidine-1-carboxylate

CAS1700611-18-2

pharmaceutical intermediate

Referencestereoisomer of

Tert-butyl (3R,4R)-3-amino-4-fluoropiperidine-1-carboxylate

CAS1932499-00-7

pharmaceutical intermediate

Referencestereoisomer of

Tert-butyl (3R,4R)-3-amino-4-fluoropiperidine-1-carboxylate

CAS1273567-30-8

pharmaceutical intermediate

Safety Reference

Corrosive
Corrosive
Harmful
Harmful
Danger
H302Harmful if swallowed
H315Causes skin irritation
H318Causes serious eye damage
H335May cause respiratory irritation
Identifiers
IUPAC Name

tert-butyl (3S,4R)-3-amino-4-fluoropiperidine-1-carboxylate

InChIKey

CVHJEFDRBTZVEL-SFYZADRCSA-N

SMILES

CC(C)(C)OC(=O)N1CC[C@H]([C@H](C1)N)F

Synonyms (12)

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