510772-10-8

Basic information

• Product Name: Benzaldehyde, 4-(azidomethyl)-
• CAS NO: 510772-10-8
• Molecular Formula: C8H7N3O
• Molecular Weight: 161.163
• Mol File: 510772-10-8.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 4-(azidomethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 4-(azidomethyl)-(510772-10-8)
• EPA Substance Registry System: Benzaldehyde, 4-(azidomethyl)-(510772-10-8)

Safety Data

• Hazardous Substances Data: 510772-10-8(Hazardous Substances Data)

Upstream product

• 51359-78-5 4-(bromomethyl)benzaldehyde 
• 17201-43-3 4-cyanobenzyl bromide 
• 125734-44-3 4-(hydroxymethyl)benzaldehyde diethyl acetal 
• 52010-97-6 4-(hydroxylmethyl)benzaldehyde 
• 104-85-8 para-methylbenzonitrile 
• 439691-96-0 [4-(azidomethyl)phenyl]methanol 

Downstream Products

• 1049800-38-5 (E)-2-(1-(4-(azidomethyl)benzylidene)-5-fluoro-1H-inden-3-yl)-ethanoic acid 
• 1362456-41-4 1,9-diformyl-5-[4-(azidomethyl)phenyl]dipyrromethane 
• 1362456-40-3 5-[4-(azidomethyl)phenyl]dipyrromethane 
• 1372135-67-5 5-(4-(azidomethyl)phenyl)-10,15,20-tritolylporphyrin zinc 
• 156866-52-3 tert-butyl N-(4-formylbenzyl)carbamate 
• 439691-96-0 [4-(azidomethyl)phenyl]methanol 
• 39895-56-2 4-hydroxymethyl-benzylamine 
• 1385773-93-2 2-(t-butoxycarbonylamino)ethyl 3-N-(4-(azidomethyl)benzyl)-aminopropyl ether 
• 1385773-94-3 2-aminoethyl 3-N-(4-(azidomethyl)benzyl)-aminopropyl ether 
• 1385773-95-4 2-(pyren-1-ylmethylamino)ethyl 3-N-(4-(azidomethyl)benzyl)-aminopropyl ether 
• 1385773-96-5 (N-(pyren-1-ylmethyl)-N-(benzyl-2-boronic acid)-aminoethyl) (N'-(4-(azidomethyl)benzyl)-N'-(benzyl-2'-boronic acid)-3-aminopropyl)ether 
• 123986-64-1 tert-butyl 4-hydroxymethylbenzylcarbamate 

Relevant articles and documents

Isoselective Lactide Ring Opening Polymerisation using [2]Rotaxane Catalysts

Polylactide (PLA) is a fully biodegradable and recyclable plastic, produced from a bio-derived monomer: it is a circular economy plastic. Its properties depend upon its stereochemistry and isotactic PLA shows superior thermal-mechanical performances. Here, a new means to control tacticity by exploiting rotaxane conformational dynamism is described. Dynamic achiral [2]rotaxanes can show high isoselectivity (Pi=0.8, 298 K) without requiring any chiral additives and enchain by a chain end control mechanism. The organocatalytic dynamic stereoselectivity is likely applicable to other small-molecule and polymerization catalyses.

Redox reaction between benzyl azides and aryl azides: concerted synthesis of aryl nitriles and anilines

A unique and novel reaction between benzyl azides and aryl azides is described to synthesize aryl nitriles and anilines concurrently, which is catalyzed with a photoactivated diruthenium complex. N-Unsubstituted imines (N-H imines) are generated first from benzyl azides, followed by the hydrogen transfer reaction between N-H imines and aryl azides. A wide range of aryl nitriles and anilines were synthesized under neutral and mild reaction conditions.

Porphyrin-functionalized mesoporous organosilica nanoparticles for two-photon imaging of cancer cells and drug delivery

The synthesis of a zinc porphyrin derivative possessing eight triethoxysilyl groups was performed through a CuAAC-click reaction. This porphyrin was covalently entrapped in ethenylene-bridged mesoporous organosilica nanoparticles which efficiently allowed