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ChemicalBook > Product Catalogue >Organic Chemistry >Amides >Acyclic polyamines and their derivatives >2,6-Dioxopiperidine-3-ammonium chloride

2,6-Dioxopiperidine-3-ammonium chloride

2,6-Dioxopiperidine-3-ammonium chloride Structure
  • ₹0
  • Product name: 2,6-Dioxopiperidine-3-ammonium chloride
  • CAS: 24666-56-6
  • MF: C5H9ClN2O2
  • MW: 164.59016
  • EINECS:807-866-6
  • MDL Number:MFCD11042437
  • Synonyms:2,6-Dioxopiperidine-3-ammonium chloride;2,6-Dioxopiperidine-3-ammonium;Lenalidomide Impurity 6 HCl;Pomalidomide/lenalidomide INT II;3-Amino-piperidine-2,6-dione [2353-44-8] at 262 USD, please be noted, what we provide is HCl salt form;2,6-dioxopiperidin-3-aminium chloride;Pomalidomide Impurity 6;6-piperidinedione hydrochloride
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

Melting point :120 °C (approx)
storage temp. :Inert atmosphere,Room Temperature
solubility :DMSO (Slightly, Heated), Methanol (Sparingly, Sonicated)
form :powder
color :White
InChI :InChI=1S/C5H8N2O2.ClH/c6-3-1-2-4(8)7-5(3)9;/h3H,1-2,6H2,(H,7,8,9);1H
InChIKey :YCPULGHBTPQLRH-UHFFFAOYSA-N
SMILES :C1CC(N)C(=O)NC1=O.Cl

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H315 Causes skin irritation Skin corrosion/irritation Category 2 Warning GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 Causes serious eye irritation Serious eye damage/eye irritation Category 2A Warning GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 May cause respiratory irritation Specific target organ toxicity, single exposure;Respiratory tract irritation Category 3 Warning GHS hazard pictograms
Precautionary statements:
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P271 Use only outdoors or in a well-ventilated area.
P280 Wear protective gloves/protective clothing/eye protection/face protection.

Description

2,6-Dioxopiperidine-3-ammonium chloride is a reagent for preparing lenalidomide that can induce ubiquitination and degradation of CK1α in del (5q) MDS. It can also be used to prepare phthalimide conjugates that can promote ligand-dependent target protein degradation. Moreover, it is also a metabolite of thalidomide (T338850) that inhibits FGF-induced angiogenesis.

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