518522
1-Piperidinecarbonyl chloride
97%
Synonym(s):
N-Chloroformylpiperidine, NSC 50227
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About This Item
Empirical Formula (Hill Notation):
C6H10ClNO
CAS Number:
Molecular Weight:
147.60
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
97%
refractive index
n20/D 1.459 (lit.)
bp
242 °C (lit.)
density
1.18 g/mL at 25 °C (lit.)
functional group
chloro
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
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
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
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
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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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