| Dibenzyl azodicarboxylate Basic information |
| Product Name: | Dibenzyl azodicarboxylate |
| Synonyms: | Dibenzy| azodicarbo×ylate;diazenedicarboxylicacid,bis(phenylmethyl)ester;Phenylmethyl N-(phenylmethoxycarbonylimino)carbamate;Dibenzyl Azodicarboxylate (40% in Dichloromethane, ca. 1.7mol/L);Azobis(formic acid benzyl) ester;Azodiformic acid dibenzyl ester;Bis(benzyloxycarbonyl)diazene;Diazene-1,2-dicarboxylic acid dibenzyl ester |
| CAS: | 2449-05-0 |
| MF: | C16H14N2O4 |
| MW: | 298.29 |
| EINECS: | 219-508-0 |
| Product Categories: | Aromatic Esters;Azo/Diazo Compounds;Nitrogen Compounds;Organic Building Blocks |
| Mol File: | 2449-05-0.mol |
| Dibenzyl azodicarboxylate Chemical Properties |
| Melting point | 43-47 °C (lit.) |
| Boiling point | 439.72°C (rough estimate) |
| density | 1.2028 (rough estimate) |
| refractive index | 1.6240 (estimate) |
| Fp | >230 °F |
| storage temp. | 2-8°C |
| form | Crystalline Powder |
| color | Yellow to orange |
| Sensitive | Light Sensitive |
| BRN | 2298734 |
| InChIKey | IRJKSAIGIYODAN-ISLYRVAYSA-N |
| CAS DataBase Reference | 2449-05-0(CAS DataBase Reference) |
| EPA Substance Registry System | Diazenedicarboxylic acid, bis(phenylmethyl) ester (2449-05-0) |
| Safety Information |
| Hazard Codes | Xi,F |
| Risk Statements | 36/37/38-11 |
| Safety Statements | 26-37/39-16 |
| RIDADR | 3224 |
| WGK Germany | 3 |
| TSCA | Yes |
| HS Code | 29270000 |
| MSDS Information |
| Provider | Language |
|---|---|
| Dibenzyl azodicarboxylate | English |
| SigmaAldrich | English |
| ACROS | English |
| ALFA | English |
| Dibenzyl azodicarboxylate Usage And Synthesis |
| Chemical Properties | yellow to orange crystalline powder |
| Uses | Dibenzyl azodicarboxylate is a reagent used in the synthesis of Minocycline-d6 (M344797). Minocycline-d6 is a labeled second generation tetracycline antibiotic. Antibacterial. |
| Uses | Dibenzyl azodicarboxylate was used as electrophilic reagent in the synthesis of C-glycosyl α-amino acids via proline-catalyzed α-amination of C-glycosylalkyl aldehydes. It was used in enantioselective synthesis of optically active pyrazolidine derivatives. |
| General Description | Dibenzyl azodicarboxylate undergoes[4+2] cycloaddition reaction with glycal to yield 2-aminoglycosides. |
| Dibenzyl azodicarboxylate Preparation Products And Raw materials |
| Raw materials | 1,2-DICARBOBENZYLOXYHYDRAZINE |
Please leave a message for us or use the following ways to contact us, we will reply to you as soon as possible, and provide you with the most sincere service, thank you.
日本语
한국어
Français
Deutsch
España
Türkiye