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Azidomethyl 2,2-dimethylpropanoate

Base Information
  • Chemical Name:Azidomethyl 2,2-dimethylpropanoate
  • CAS No.:872700-68-0
  • Molecular Formula:C6H11N3O2
  • Molecular Weight:157.172
  • Hs Code.:
  • European Community (EC) Number:694-548-3
  • Nikkaji Number:J2.916.892J
Azidomethyl 2,2-dimethylpropanoate

Synonyms:Azidomethyl 2,2-dimethylpropanoate;872700-68-0;azidomethyl pivalate;Propanoic acid, 2,2-dimethyl-, azidomethyl ester;Azidomethyl pivalate, 97%;SCHEMBL13464950;MEJGIRNNNFPMOX-UHFFFAOYSA-N;2,2-dimethylpropionic acid azidomethyl ester;EN300-257496

Suppliers and Price of Azidomethyl 2,2-dimethylpropanoate
Supply Marketing:
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
  • Sigma-Aldrich
  • Azidomethyl pivalate 97%
  • 5g
  • $ 114.00
Total 2 raw suppliers
Chemical Property of Azidomethyl 2,2-dimethylpropanoate
Chemical Property:
  • Refractive Index:n20/D1.428 
  • Flash Point:59℃ 
  • PSA:76.05000 
  • Density:1.026 g/mL at 25 °C 
  • LogP:1.29626 
  • XLogP3:2.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:157.085126602
  • Heavy Atom Count:11
  • Complexity:189
Purity/Quality:

97% *data from raw suppliers

Azidomethyl pivalate 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)C(=O)OCN=[N+]=[N-]
Technology Process of Azidomethyl 2,2-dimethylpropanoate

There total 1 articles about Azidomethyl 2,2-dimethylpropanoate 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 sodium azide; In water; at 90 ℃; for 18h;
DOI:10.1002/asia.201800452
Guidance literature:
With copper(II) sulfate; sodium L-ascorbate; In water; tert-butyl alcohol; at 20 ℃; for 12h; regioselective reaction;
DOI:10.1021/ol101082v
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