Dibenzyl-(E)-diazen-1,2-dicarboxylat
Names
[ CAS No. ]:
2449-05-0
[ Name ]:
Dibenzyl-(E)-diazen-1,2-dicarboxylat
[Synonym ]:
Dibenzyl azodicarbox
EINECS 219-508-0
dibenzyl diazodicarboxylate
Azodicarboxylic Acid Dibenzyl Ester
Dibenzyl Azodicarboxylate
Dibenzyl (E)-diazene-1,2-dicarboxylate
Azodiformic acid dibenzyl ester
dibenzyl diazenedicarboxylate
Dibenzyl diazene-1,2-dicarboxylate
MFCD00016737
di-benzyl azodicarboxylate
1,2-Diazenedicarboxylic acid, bis(phenylmethyl) ester, (E)-
Dibenzyl-(E)-diazen-1,2-dicarboxylat
Dibenzyl (E)-1,2-diazenedicarboxylate
DBAD
Chemical & Physical Properties
[ Density]:
1.2±0.1 g/cm3
[ Boiling Point ]:
456.8±34.0 °C at 760 mmHg
[ Melting Point ]:
43-47 °C(lit.)
[ Molecular Formula ]:
C16H14N2O4
[ Molecular Weight ]:
298.293
[ Flash Point ]:
203.0±20.1 °C
[ Exact Mass ]:
298.095367
[ PSA ]:
77.32000
[ LogP ]:
4.34
[ Vapour Pressure ]:
0.0±1.1 mmHg at 25°C
[ Index of Refraction ]:
1.568
[ Storage condition ]:
0-6°C
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
F:Flammable;Xi:Irritant;
[ Risk Phrases ]:
R11;R36/37/38
[ Safety Phrases ]:
S26-S37/39-S16
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2927000090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2927000090
[ Summary ]:
2927000090 other diazo-, azo- or azoxy-compounds。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%
Articles
Org. Lett. 6(13) , 2193-6, (2004)
[reaction: see text] Optically active pyrazolidine derivatives have been constructed by the Cu- and Pd-catalyzed asymmetric one-pot tandem addition-cyclization reaction of 2-(2',3'-dienyl)-beta-ketoes...
General synthesis of C-glycosyl amino acids via proline-catalyzed direct electrophilic alpha-amination of C-glycosylalkyl aldehydes.Org. Lett. 10(20) , 4485-8, (2008)
Non-natural axially and equatorially linked C-glycosyl alpha-amino acids (glycines, alanines, and CH2-serine isosteres) with either S or R alpha-configuration were prepared by D- and L-proline-catalyz...
[4+ 2] Cycloaddition reaction of dibenzyl azodicarboxylate and glycals. Leblanc Y, et al.J. Am. Chem. Soc. 111(8) , 2995-3000, (1989)