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518522

Sigma-Aldrich

1-Piperidinecarbonyl chloride

97%

Synonym(s):

N-Chloroformylpiperidine, NSC 50227

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About This Item

Empirical Formula (Hill Notation):
C6H10ClNO
CAS Number:
13939-69-0
Molecular Weight:
147.60
MDL number:
MFCD00973554
UNSPSC Code:
12352100
PubChem Substance ID:
24874029
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.459 (lit.)

bp

242 °C (lit.)

density

1.18 g/mL at 25 °C (lit.)

SMILES string

ClC(=O)N1CCCCC1

InChI

1S/C6H10ClNO/c7-6(9)8-4-2-1-3-5-8/h1-5H2

InChI key

BIFDXOOJPDHKJH-UHFFFAOYSA-N

Related Categories

Application

Reactant for synthesis of:
A coumarin-based HIV-1 Vpr inhibitor
Antitumor agents as potent chemosensitizers
Oxime carbamates as reversible inhibitors of fatty acid amide hydrolase
Dipeptidyl peptidase 4 inhibitors for the treatment of type 2 diabetes
Bisarylmaleimide glycogen synthase kinase-3 inhibitors
Lysosomal acid lipase inhibitors and potential Niemann-Pick type C disease therapeutics

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

518522-VAR:
518522-BULK:
518522-5G:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Correlation of the rates of solvolysis of 1-piperidincarbonyl chloride using the extended Grunwald-Winstein equation.
Choi H, et al.
Bull. Korean Chem. Soc., 32(11), 3941-3941 (2011)
Self-assembling decacyclene triimides prepared through a regioselective hextuple Friedel-Crafts carbamylation.
Toan V Pho et al.
Angewandte Chemie (International ed. in English), 52(5), 1446-1451 (2012-12-21)
Jure Borišek et al.
Journal of medicinal chemistry, 58(17), 6928-6937 (2015-08-19)
Cathepsin K is a major drug target for osteoporosis and related-bone disorders. Using a combination of virtual combinatorial chemistry, QSAR modeling, and molecular docking studies, a series of cathepsin K inhibitors based on N-(functionalized benzoyl)-homocycloleucyl-glycinonitrile scaffold was developed. In order
New nordihydroguaiaretic acid derivatives as anti-HIV agents.
Hwu JR, et al.
Bioorganic & Medicinal Chemistry Letters, 18(6), 1884-1888 (2008)

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