1-PIPERIDINECARBONYL CHLORIDE

1-PIPERIDINECARBONYL CHLORIDE Basic information
Product Name:1-PIPERIDINECARBONYL CHLORIDE
Synonyms:1-PIPERIDINECARBONYL CHLORIDE;N-Piperidinecarbonyl chloride;1-Piperidinecarbonyl chloride (6CI,7CI,8CI,9CI);N-Chloroformylpiperidine;NSC 50227;piperidine-1-carbonyl chloride;1-Piperidinecarbonyl chloride 97%;1-(Chlorocarbonyl)piperidine
CAS:13939-69-0
MF:C6H10ClNO
MW:147.6
EINECS:
Product Categories:ACIDHALIDE;Building Blocks;Heterocyclic Building Blocks;Piperidines;Building Blocks;C5 to C7;Chemical Synthesis;Heterocyclic Building Blocks
Mol File:13939-69-0.mol
1-PIPERIDINECARBONYL CHLORIDE Structure
1-PIPERIDINECARBONYL CHLORIDE Chemical Properties
Boiling point 242 °C (lit.)
density 1.18 g/mL at 25 °C (lit.)
refractive index n20/D 1.459(lit.)
Fp 110 °C
pka-1.85±0.20(Predicted)
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-27-36/37/39-45
RIDADR UN 3265 8/PG 3
WGK Germany 3
HS Code 2933399990
MSDS Information
ProviderLanguage
SigmaAldrich English
1-PIPERIDINECARBONYL CHLORIDE Usage And Synthesis
UsesReactant for synthesis of: A coumarin-based HIV-1 Vpr inhibitor1 Antitumor agents as potent chemosensitizers2 Oxime carbamates as reversible inhibitors of fatty acid amide hydrolase3 Dipeptidyl peptidase 4 inhibitors for the treatment of type 2 diabetes4 Bisarylmaleimide glycogen synthase kinase-3 inhibitors5 Lysosomal acid lipase inhibitors and potential Niemann-Pick type C disease therapeutics6
UsesReactant 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
1-PIPERIDINECARBONYL CHLORIDE Preparation Products And Raw materials
Preparation Products1-[1,1'-Biphenyl]-4-ylethenyl Ester 1-Piperidinecarboxylic Acid
1-Piperidinecarbonyl chloride, 3-methyl- (9CI) N-CHLOROMETHYL PIPERIDINE 1-Chlorocarbonyl-4-piperidinopiperidine hydrochloride 1-Piperidinecarbonyl chloride, 2-(2-propenyl)- (9CI) 3-Piperidinecarbonyl chloride, 1-acetyl- (9CI) 4-Piperidinecarbonyl chloride, 4-hydroxy-1-methyl- (9CI) 1-PIPERIDINECARBONYL CHLORIDE 1-CHLOROCARBONYL-4-PIPERIDINOPIPERIDINE 1-ACETYL-4-PIPERIDINECARBONYL CHLORIDE 4-Piperidinecarboxylic acid, 1-(chlorocarbonyl)-, methyl ester (9CI) 1-Piperidinecarbonyl chloride, 3-hydroxy- (9CI) 2-Piperidinecarbonyl chloride (9CI) 3α-Methyl-1-[(4-methylphenyl)sulfonyl]-4-phenyl-4β-piperidinecarbonyl chloride Ethylmethyl-carbamic chloride Dimethylcarbamoyl chloride Diethylcarbamyl chloride 3-Piperidinecarbonyl chloride, 1-(aminoiminomethyl)- (9CI) carbamoyl chloride

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