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(2S)-2-tert-Butyloxy-butanedioic Acid tert-Butyl Ethyl Ester

Base Information Edit
  • Chemical Name:(2S)-2-tert-Butyloxy-butanedioic Acid tert-Butyl Ethyl Ester
  • CAS No.:958350-60-2
  • Molecular Formula:C14H26O5
  • Molecular Weight:274.357
  • Hs Code.:
  • Mol file:958350-60-2.mol
(2S)-2-tert-Butyloxy-butanedioic Acid tert-Butyl Ethyl Ester

Synonyms:

Suppliers and Price of (2S)-2-tert-Butyloxy-butanedioic Acid tert-Butyl Ethyl Ester
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • (2S)-2-tert-Butyloxy-butanedioicAcidtert-ButylEthylEster
  • 1g
  • $ 1320.00
  • Medical Isotopes, Inc.
  • (2S)-2-tert-Butyloxy-butanedioicAcidtert-ButylEthylEster
  • 1 g
  • $ 2200.00
Total 0 raw suppliers
Chemical Property of (2S)-2-tert-Butyloxy-butanedioic Acid tert-Butyl Ethyl Ester Edit
Chemical Property:
  • Solubility.:Dichloromethane, Ethyl Acetate 
Purity/Quality:

(2S)-2-tert-Butyloxy-butanedioicAcidtert-ButylEthylEster *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses (2S)-2-tert-Butyloxy-butanedioic Acid tert-Butyl Ethyl Ester is a reactant used in the preparation of 2’-Deoxymugineic Acid (D243250). A reactant used in the preparation of 2’-Deoxymugineic Acid (D243250).
Technology Process of (2S)-2-tert-Butyloxy-butanedioic Acid tert-Butyl Ethyl Ester

There total 3 articles about (2S)-2-tert-Butyloxy-butanedioic Acid tert-Butyl Ethyl Ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
isobutene; (S)-4-ethoxy-2-hydroxy-4-oxobutanoic acid; In dichloromethane; for 0.0333333h; Inert atmosphere;
With sulfuric acid; In dichloromethane; at 20 ℃; for 4h; Inert atmosphere; Sealed tube;
DOI:10.1002/chem.202004004
Guidance literature:
Multi-step reaction with 2 steps
1.1: acetic acid / water / 1.5 h / 100 °C
2.1: dichloromethane / 0.03 h / Inert atmosphere
2.2: 4 h / 20 °C / Inert atmosphere; Sealed tube
With acetic acid; In dichloromethane; water;
DOI:10.1002/chem.202004004
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