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Di-t-butyl diazomalonate

Base Information
  • Chemical Name:Di-t-butyl diazomalonate
  • CAS No.:35207-75-1
  • Molecular Formula:C11H18 N2 O4
  • Molecular Weight:242.275
  • Hs Code.:2927000090
  • European Community (EC) Number:851-737-7
  • DSSTox Substance ID:DTXSID60450966
  • Nikkaji Number:J437.086D
  • NSC Number:138650
  • Mol file:35207-75-1.mol
Di-t-butyl diazomalonate

Synonyms:di-t-butyl diazomalonate;35207-75-1;ditert-butyl 2-diazopropanedioate;NSC 138650;1,3-DI-TERT-BUTYL 2-DIAZOPROPANEDIOATE;di-t-butyl-2-diazomalonate;SCHEMBL7786553;DTXSID60450966;RXYMTVAHQNMICF-UHFFFAOYSA-N;NSC138650;NSC-138650;EN300-6504431;(1E)-1,3-Di-tert-butoxy-2-diazonio-3-oxoprop-1-en-1-olate

Suppliers and Price of Di-t-butyl diazomalonate
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
Total 5 raw suppliers
Chemical Property of Di-t-butyl diazomalonate
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:89.99000 
  • Density:g/cm3 
  • LogP:1.42166 
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:6
  • Exact Mass:242.12665706
  • Heavy Atom Count:17
  • Complexity:338
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)OC(=O)C(=[N+]=[N-])C(=O)OC(C)(C)C
Technology Process of Di-t-butyl diazomalonate

There total 6 articles about Di-t-butyl diazomalonate 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 4-toluenesulfonyl azide; caesium carbonate; In tetrahydrofuran; for 1h; Ambient temperature;
DOI:10.1080/00397919508011762
Guidance literature:
With triethylamine; In acetonitrile; at 20 ℃; Inert atmosphere;
DOI:10.1002/anie.202007176
Guidance literature:
With sodium hydroxide; In 1,2-dichloro-ethane; for 6h; Ambient temperature;
DOI:10.1080/00397919108055444
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