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ChemicalBook > Product Catalogue >Organic Chemistry >Carboxylic acids and derivatives >Carboxylic acid halides >1-PIPERIDINECARBONYL CHLORIDE

1-PIPERIDINECARBONYL CHLORIDE

1-PIPERIDINECARBONYL CHLORIDE Structure
  • ₹8140.4
  • Product name: 1-PIPERIDINECARBONYL CHLORIDE
  • CAS: 13939-69-0
  • MF: C6H10ClNO
  • MW: 147.6
  • EINECS:
  • MDL Number:MFCD00973554
  • Synonyms:1-PIPERIDINECARBONYL CHLORIDE;N-Piperidinecarbonyl chloride ;1-Piperidinecarbonyl chloride (6CI,7CI,8CI,9CI);N-Chloroformylpiperidine;NSC 50227;1-Piperidinecarbonyl chloride 97%;1-(Chlorocarbonyl)piperidine;1-piperidinyl chloride
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Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 5G
  • ManufacturerSigma-Aldrich(India)
  • Product number518522
  • Product description1-Piperidinecarbonyl chloride 97%
  • Packaging5G
  • Price₹8140.4
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) 518522 1-Piperidinecarbonyl chloride 97% 5G ₹8140.4 2022-06-14 Buy

Properties

Boiling point :242 °C (lit.)
Density :1.18 g/mL at 25 °C (lit.)
refractive index :n20/D 1.459(lit.)
Flash point :110 °C
pka :-1.85±0.20(Predicted)

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Danger
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H314 Causes severe skin burns and eye damage Skin corrosion/irritation Category 1A, B, C Danger GHS hazard pictograms P260,P264, P280, P301+P330+ P331,P303+P361+P353, P363, P304+P340,P310, P321, P305+ P351+P338, P405,P501
Precautionary statements:
P280 Wear protective gloves/protective clothing/eye protection/face protection.
P303+P361+P353 IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P363 Wash contaminated clothing before reuse.
P405 Store locked up.

Description

Reactant 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

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