Chemical plants supply high-quality Diethyl azodicarboxylate 1972-28-7 in bulk

Q: What is the Diethyl azodicarboxylate?

Diethyl azodicarboxylate is Clear orange to orange-red liquid, while it's Molecular Formula is C6H10N2O4. Clear orange to orange-red liquid Reactant for preparation of:Immunostimulants α-GalactosylceramidesCellotriose and cellotetraose analogues as transition state mimics for mechanistic studies of cellulasesBisubstrate inhibitors with molecular recognition at the active site of catechol-O-methyltransferaseDerivatives of F200 and S383 with cannabinoid CB1 receptor binding activitiesAza-β-lactams via NHC-catalyzed [2 + 2] cycloaddition with ketenesReagent for:Annulation of N-protected iminesα-thiocyanation of enolizable ketones with ammonium thiocyanateDiels-Alder reactions

Quality products make an important contribution to long-term revenue and profitability. Chemical plants supply high-quality Diethyl azodicarboxylate 1972-28-7 in bulk

1.What is the Diethyl azodicarboxylate ?

Clear orange to orange-red liquid

Diethyl azodicarboxylate, also known as diethyl diazene-1,2-dicarboxylate, is an organic compound with the chemical formula C6H10N2O4. It is a clear orange to orange-red liquid and is known for its use as a reagent and building block in various chemical reactions and applications.

2.What is the CAS number for Diethyl azodicarboxylate ?

The CAS number of Diethyl azodicarboxylate is 1972-28-7.

3.What are another words for Diethyl azodicarboxylate ?

Synonyms for Diethyl azodicarboxylate 1972-28-7:Diazenedicarboxylicacid, diethyl ester (9CI);Formic acid, azodi-, diethyl ester (6CI,8CI);1,2-Ethoxycarbonyl diazene;Azodicarboxylic acid diethyl ester;DEAD;Diethoxycarbonyldiazene;Diethyl azodicarboxylate;Diethyl diazenedicarboxylate;Diethyl diazodicarboxylate;NSC 3474;NSC 679015;Unifoam AZ-AE 200;

4.What is Diethyl azodicarboxylate (1972-28-7) used for?

Reactant for preparation of:Immunostimulants α-GalactosylceramidesCellotriose and cellotetraose analogues as transition state mimics for mechanistic studies of cellulasesBisubstrate inhibitors with molecular recognition at the active site of catechol-O-methyltransferaseDerivatives of F200 and S383 with cannabinoid CB1 receptor binding activitiesAza-β-lactams via NHC-catalyzed [2 + 2] cycloaddition with ketenesReagent for:Annulation of N-protected iminesα-thiocyanation of enolizable ketones with ammonium thiocyanateDiels-Alder reactions

InChI:InChI=1/C6H10N2O4/c1-5(9)11-3-7-8-4-12-6(2)10/h3-4H2,1-2H3/b8-7+

Relevant articles related to Diethyl azodicarboxylate:

Article	Source
-	Buechi et al. , p. 37,39, 40 (1962)
Synthesis and neuroprotective properties of isosteric analogs of nicotine	Matveeva,Podrugina,Morozkin,Tkachenko,Zefirov , p. 1149 - 1153 (2000)
Kinetic profiling of prolinate-catalyzed α-amination of aldehydes	Hein, Jason E.,Armstrong, Alan,Blackmond, Donna G. , p. 4300 - 4303 (2011)

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