Propanedioic acid, oxo-, bis(1-methylethyl) ester

Propanedioic acid, oxo-, bis(1-methylethyl) ester
  • CAS No.:73972-39-1

Important Notice

  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
  3. The purchaser must not use this product, or supply it to another party, for personal consumption, sports or fitness, weight loss, health supplements, food, or animal feed.
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Propanedioic acid, oxo-, bis(1-methylethyl) ester Basic information
Product Name:Propanedioic acid, oxo-, bis(1-methylethyl) ester
Synonyms:Propanedioic acid, oxo-, bis(1-methylethyl) ester;Diisopropyl 2-oxomalonate;Propanedioic acid, 2-oxo-, 1,3-bis(1-methylethyl) ester
CAS:73972-39-1
MF:C9H14O5
MW:202.2
EINECS:
Product Categories:
Mol File:73972-39-1.mol
Propanedioic acid, oxo-, bis(1-methylethyl) ester Chemical Properties
density 1.036
Safety Information
MSDS Information
Propanedioic acid, oxo-, bis(1-methylethyl) ester Usage And Synthesis
UsesAs demonstrated by Laszlo Kürti′s lab, the sterically hindered di-isopropyl keto malonate and its hydrate (902764) are excellent N-umpolung reagents for both aliphatic and aromatic primary amines via a simple condensation reaction. The steric hindrance in ester moiety allows the preparation of the corresponding iminomalonates in high yield and lends these imines sufficient hydrolytic stability during the purification process. The N-alkyl as well as N-aryl iminomalonates act as singly N-electrophilic reagents towards strong C-nucleophiles such as alkyl- and arylmetals (e.g., Grignard reagents). Thus, unsymmetrical secondary amines may be readily prepared at low temperatures and in the absence of transition metal catalysts.
Propanedioic acid, oxo-, bis(1-methylethyl) ester Preparation Products And Raw materials

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