• Product NameDiethyl azodicarboxylate
  • CasNo. 1972-28-7
  • MFC6H10N2O4
  • MW174.156
  • Purity
  • AppearanceClear orange to orange-red liquid
  • Packing
  • Contact usInquiry

Product Details

CasNo: 1972-28-7

MF: C6H10N2O4

Appearance: Clear orange to orange-red liquid

Trustworthy Factory Supply Wholesale 1972-28-7 Customized Supply

  • Molecular Formula:C6H10N2O4
  • Molecular Weight:174.156
  • Appearance/Colour:Clear orange to orange-red liquid 
  • Vapor Pressure:0.589mmHg at 25°C 
  • Melting Point:6°C 
  • Refractive Index:n20/D 1.47  
  • Boiling Point:226.3 °C at 760 mmHg 
  • Flash Point:106.9 °C 
  • PSA:77.32000 
  • Density:1.2 g/cm3 
  • LogP:1.75160 

Diethyl azodicarboxylate(Cas 1972-28-7) Usage

Chemical Description

Diethyl azodicarboxylate is a reagent used in organic synthesis to introduce azo groups.

Purification Methods

Dissolve DEAD in toluene, wash it with 10% NaHCO3 till neutral (may require several washes if too much hydrolysis had occurred: check IR for OH bands), then wash with H2O (2x), dry over Na2SO4, filter, evaporate the toluene and distil it through a short Vigreux column (p 11) at as high a vacuum as possible. The main portion boils at 107-111o/15mm. Since it is likely to explode, use an oil bath for heating the still and all operations should be carried -out behind an adequate shield. [Rabjohn Org Synth Coll Vol III 375 1955, see Kauer Org Synth Coll Vol IV 412 1963]. [Beilstein 3 III 233.] It is commercially available as a 40% solution in toluene. This reagent is useful in the Mitsunobu reaction [Mitsunobu Synthesis 1 1981, Gennari et al. J Am Chem Soc 108 6394 1986, Evans et al. J Am Chem Soc 108 6394 1986, Hughes Org React 42 335 1992, Dodge et al. Org Synth 73 110 1996, Hughes Org Prep Proc Int 28 127 1996, Ferguson & Marcelle J Am Chem Soc 128 4576 2006; see also di-tert-butyl azodicarboxylate above and DIAD below]. § A polystyrene supported DEAD version is commercially available with a loading of ~1.2mmol/g.

General Description

DOT Special Approval Submission is Under Review. Availability is Estimated as March 2012.

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

1972-28-7 Relevant articles

-

Buechi et al.

, p. 37,39, 40 (1962)

-

EFFECT OF SOLVENTS ON PHOTOLYTIC DECOMPOSITION OF ETHYL AZIDOFORMATE

Chekrygin, V. A.,Shelemina, N. V.,Nikitina, G. V.,Solnyshkina, L. I.

, p. 407 - 410 (1983)

-

Synthesis and neuroprotective properties of isosteric analogs of nicotine

Matveeva,Podrugina,Morozkin,Tkachenko,Zefirov

, p. 1149 - 1153 (2000)

A method has been developed for the synt...

Kinetic profiling of prolinate-catalyzed α-amination of aldehydes

Hein, Jason E.,Armstrong, Alan,Blackmond, Donna G.

, p. 4300 - 4303 (2011)

Deconvolution of the role of off-cycle s...

-

Reynolds,Hauser

, p. Warnungsbeilage (1958)

-

METHOD FOR PRODUCING AZO COMPOUNDS

-

Paragraph 0046, (2018/04/14)

PROBLEM TO BE SOLVED: To provide a metho...

METHOD FOR PRODUCING AZO COMPOUNDS

-

Paragraph 0050; 0051, (2018/08/22)

PROBLEM TO BE SOLVED: To provide a metho...

METHOD FOR PRODUCING AZO COMPOUNDS

-

Paragraph 0048; 0062, (2018/05/03)

PROBLEM TO BE SOLVED: To provide a metho...

Photocatalytic esterification under Mitsunobu reaction conditions mediated by flavin and visible light

M?rz,Chudoba,Kohout,Cibulka

supporting information, p. 1970 - 1975 (2017/03/11)

The usefulness of flavin-based aerial ph...

1972-28-7 Process route

4,7-Dimethyl-15-oxo-5,6-diphenyl-11,12-diazapentacyclo<8.2.2.1<sup>4,7</sup>.0<sup>2,9</sup>.0<sup>3,8</sup>>pentadeca-5,13-dien-11,12-dicarbonsaeure-diethylester
73240-57-0,77881-55-1

4,7-Dimethyl-15-oxo-5,6-diphenyl-11,12-diazapentacyclo<8.2.2.14,7.02,9.03,8>pentadeca-5,13-dien-11,12-dicarbonsaeure-diethylester

diethyl hydrazodicarboxylate
4114-28-7

diethyl hydrazodicarboxylate

methyl 3',6'-dimethyl[1,1*:2',1-terphenyl]-4'-carboxylate
13102-23-3

methyl 3',6'-dimethyl[1,1*:2',1-terphenyl]-4'-carboxylate

4,9-Dimethyl-6,7-diphenyl-5,8-dioxa-13,14-diazahexacyclo<10.2.2.0<sup>2,11</sup>.0<sup>3,10</sup>.0<sup>4,6</sup>.0<sup>7,9</sup>>hexadec-15-en-13,14-dicarbonsaeure-diethylester
86814-76-8

4,9-Dimethyl-6,7-diphenyl-5,8-dioxa-13,14-diazahexacyclo<10.2.2.02,11.03,10.04,6.07,9>hexadec-15-en-13,14-dicarbonsaeure-diethylester

diethylazodicarboxylate
1972-28-7,218603-74-8

diethylazodicarboxylate

Conditions
Conditions Yield
In diethyl ether; acetone; at -25 - -20 ℃; for 6h; Irradiation;
46%
7%
4,7-Dimethyl-15-oxo-5,6-diphenyl-11,12-diazapentacyclo<8.2.2.1<sup>4,7</sup>.0<sup>2,9</sup>.0<sup>3,8</sup>>pentadeca-5,13-dien-11,12-dicarbonsaeure-diethylester
73240-57-0,77881-55-1

4,7-Dimethyl-15-oxo-5,6-diphenyl-11,12-diazapentacyclo<8.2.2.14,7.02,9.03,8>pentadeca-5,13-dien-11,12-dicarbonsaeure-diethylester

diethyl hydrazodicarboxylate
4114-28-7

diethyl hydrazodicarboxylate

methyl 3',6'-dimethyl[1,1*:2',1-terphenyl]-4'-carboxylate
13102-23-3

methyl 3',6'-dimethyl[1,1*:2',1-terphenyl]-4'-carboxylate

4,9-Dimethyl-6,7-diphenyl-5,8-dioxa-13,14-diazahexacyclo<10.2.2.0<sup>2,11</sup>.0<sup>3,10</sup>.0<sup>4,6</sup>.0<sup>7,9</sup>>hexadec-15-en-13,14-dicarbonsaeure-diethylester
86814-76-8

4,9-Dimethyl-6,7-diphenyl-5,8-dioxa-13,14-diazahexacyclo<10.2.2.02,11.03,10.04,6.07,9>hexadec-15-en-13,14-dicarbonsaeure-diethylester

diethylazodicarboxylate
1972-28-7,218603-74-8

diethylazodicarboxylate

benzene
71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1

benzene

Conditions
Conditions Yield
In diethyl ether; acetone; at -25 - -20 ℃; for 6h; Product distribution; Irradiation;
46%
7%

1972-28-7 Upstream products

  • 5311-96-6
    5311-96-6

    diethyl hydrazinedicarboxylate

  • 4114-28-7
    4114-28-7

    diethyl hydrazodicarboxylate

  • 71-43-2
    71-43-2

    benzene

  • 817-87-8
    817-87-8

    ethyl azidocarbonate

1972-28-7 Downstream products

  • 10465-81-3
    10465-81-3

    1,1'-(Azodicarbonyl)dipiperidin

  • 54660-01-4
    54660-01-4

    (N-methyl-anilinomethyl)-hydrazine-N,N'-dicarboxylic acid diethyl ester

  • 298-12-4
    298-12-4

    Glyoxilic acid

  • 116838-28-9
    116838-28-9

    2,2'-diphenyl-[3,3']biindolylidene 1,1'-dioxide

Relevant Products