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2-Methylpropanoate

Base Information
  • Chemical Name:2-Methylpropanoate
  • CAS No.:5711-69-3
  • Molecular Formula:C4H7O2-
  • Molecular Weight:87.0984
  • Hs Code.:
  • DSSTox Substance ID:DTXSID201295917
  • Nikkaji Number:J1.914.708H
  • Wikidata:Q27104639
2-Methylpropanoate

Synonyms:2-Methylpropanoate;Isobutyrate;2-Methylpropionate;Propanoic acid, 2-methyl-, ion(1-);5711-69-3;i-butyrate;iso-Butyrate;CHEMBL1762641;Isobutyrat;isobutric acid;iPrCO2 anion;isobutyric acid anion;CHEBI:48944;DTXSID201295917;BDBM50340058;STL483478;Q27104639

Suppliers and Price of 2-Methylpropanoate
Supply Marketing:
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 2-Methylpropanoate
Chemical Property:
  • PSA:40.13000 
  • Density:1.57g/cm3 
  • LogP:-0.60770 
  • XLogP3:1.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:0
  • Exact Mass:87.044604462
  • Heavy Atom Count:6
  • Complexity:51.1
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)C(=O)[O-]
Technology Process of 2-Methylpropanoate

There total 5 articles about 2-Methylpropanoate 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:
With hydrogen; at 37 ℃; Product distribution; Microbiological reaction;
DOI:10.1016/S0043-1354(98)00409-6
Guidance literature:
With 2,6-dimethylpyridine; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; In ethanol; dichloromethane; water; at 25 ℃; Kinetics; Thermodynamic data;
DOI:10.1002/ejoc.201301574
Guidance literature:
With C60H42N2O18(4-)*4Na(1+); water; In aq. phosphate buffer; at 25 ℃; pH=11.9; Kinetics;
DOI:10.1039/c9cc00762h
Refernces

The oxidation of Ni(ii) N-confused porphyrins (NCPs) with azo radical initiators and an unexpected intramolecular nucleophilic substitution reaction via a proposed Ni(iii) NCP intermediate

10.1039/b904615a

The study focuses on the oxidation of Ni(II) N-confused porphyrins (NCPs) using azo radical initiators, which leads to an unexpected intramolecular nucleophilic substitution reaction via a proposed Ni(III) NCP intermediate. The main chemicals used in the study include Ni(II) NCPs, azo radical initiators such as AIBN (2,2'-azobisisobutyronitrile), dimethyl 2,2'-azobis(2-methylpropionate), and diethyl 2,2'-azobis(2-methylpropionate). These chemicals serve the purpose of oxidizing Ni(II) NCPs to Ni(III) NCPs, which are key intermediates in many chemical reactions and have biological significance in enzyme-catalyzed reactions. The study aims to understand the role of nickel in these enzymes and to model nickel biosites synthetically, which could help in investigating the precise function of the nickel ion in biological processes. The research also explores the stability and reactivity of Ni(III) NCPs, which are rare and usually unstable, and the results provide insights into the oxidative chemistry of Ni(II) porphyrins and the potential applications of Ni(III) NCPs in biomimetic nickel chemistry.

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