1-Boc-4-chloropiperidine, 98%

Name: 1-Boc-4-chloropiperidine, 98% | 154874-94-9
Brand: J&K Chemical
SKU: JK541449_25_G
Price: 242.7 USD
Availability: OutOfStock

Cat. No JK541449_25_G

Vendor: J&K Chemical

Product Information

Product Name

1-Boc-4-chloropiperidine, 98%

Brand Name

J&K

Product Number

541449

CAS

154874-94-9

Molecular Formula

C10H18ClNO2

Molecular Weight

219.71

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

Tert-Butyl 4-chloropiperidine-1-carboxylate
N-Boc-4-chloropiperidine

PubChem CID

11138624

IUPAC Name

tert-butyl 4-chloropiperidine-1-carboxylate

InChI Key

NZZWXABIGMMKQL-UHFFFAOYSA-N

SMILES

CC(C)(C)OC(=O)N1CCC(CC1)Cl

Properties

Density

1.111

Boiling Point

289.7

Safety Information

Storage Condition

Room temperature

References Data Source From Pubchem

Iron-Catalyzed Borylation and Silylation of Alkyl Electrophiles

Publication Name: Science of Synthesis

Publication Date: 2023

C–H Bond Functionalization of Amines: A Graphical Overview of Diverse Methods

Publication Name: SynOpen (2017)

Publication Date: 2021-07

DOI: 10.1055/s-0040-1706051

Proline Methanologues: Design, Synthesis, Structural Properties, and Applications in Medicinal Chemistry

Publication Name: Topics in Heterocyclic Chemistry

Publication Date: 2015

DOI: 10.1007/7081_2015_191

A User-Friendly Procedure for the Preparation of Secondary Alkyl Chlorides

Publication Name: Synthesis

Publication Date: 2012-12-19

DOI: 10.1055/s-0032-1317927

Ring Contraction of 1-tert-Butoxycarbonyl-4-chloro-2-lithiopiperidine to a Cyclopropyl Intermediate, Followed by Deprotonation and Electrophilic Substitution

Publication Name: Science of Synthesis

Publication Date: 2006

1-Boc-4-chloropiperidine, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Iron-Catalyzed Borylation and Silylation of Alkyl Electrophiles

C–H Bond Functionalization of Amines: A Graphical Overview of Diverse Methods

Proline Methanologues: Design, Synthesis, Structural Properties, and Applications in Medicinal Chemistry

A User-Friendly Procedure for the Preparation of Secondary Alkyl Chlorides

Ring Contraction of 1-tert-Butoxycarbonyl-4-chloro-2-lithiopiperidine to a Cyclopropyl Intermediate, Followed by Deprotonation and Electrophilic Substitution