Dibenzyl-(E)-diazen-1,2-dicarboxylat

Modify Date: 2024-01-02 12:29:42

Dibenzyl-(E)-diazen-1,2-dicarboxylat Structure
Dibenzyl-(E)-diazen-1,2-dicarboxylat structure
Common Name Dibenzyl-(E)-diazen-1,2-dicarboxylat
CAS Number 2449-05-0 Molecular Weight 298.293
Density 1.2±0.1 g/cm3 Boiling Point 456.8±34.0 °C at 760 mmHg
Molecular Formula C16H14N2O4 Melting Point 43-47 °C(lit.)
MSDS Chinese USA Flash Point 203.0±20.1 °C
Symbol GHS07
GHS07
Signal Word Warning

 Names

Name Dibenzyl azodicarboxylate
Synonym More Synonyms

 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

 Safety Information

Symbol GHS07
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

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Dibenzyl-(E)-diazen-1,2-dicarboxylat Structure

Dibenzyl-(E)-di...

CAS#:2449-05-0

Literature: Journal of the Chemical Society, , p. 2089,2093

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Dibenzyl-(E)-diazen-1,2-dicarboxylat Structure

Dibenzyl-(E)-di...

CAS#:2449-05-0

Literature: Journal of the Chemical Society, , p. 2089,2093

 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%

 Articles3

More Articles
Cu- and Pd-catalyzed asymmetric one-pot tandem addition-cyclization reaction of 2-(2',3'-alkadienyl)-beta-keto esters, organic halides, and dibenzyl azodicarboxylate: an effective protocol for the enantioselective synthesis of pyrazolidine derivatives.

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)

 Synonyms

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
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