24173-36-2

Basic information

• Product Name: p-azidobenzaldehyde
• Synonyms: p-azidobenzaldehyde;Benzaldehyde, 4-azido-;Einecs 246-060-3
• CAS NO: 24173-36-2
• Molecular Formula: C₇H₅N₃O
• Molecular Weight: 147.1341
• EINECS: 246-060-3
• Product Categories: Aromatics, Miscellaneous Reagents
• Mol File: 24173-36-2.mol
• Article Data: 46

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: p-azidobenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: p-azidobenzaldehyde(24173-36-2)
• EPA Substance Registry System: p-azidobenzaldehyde(24173-36-2)

Safety Data

• Hazardous Substances Data: 24173-36-2(Hazardous Substances Data)

Usage

Uses

p-azidobenzaldehyde is used in the synthesis of fullerenes, and photocrosslinkable chitosans.

Upstream product

• 31499-54-4 4-azidobenzyl alcohol 
• 1304513-31-2 C₁₉H₂₀N₄O₃ 
• 1304513-34-5 C₂₆H₂₃N₅O₇ 
• 1304513-35-6 C₂₆H₂₅N₅O₉ 
• 1304513-32-3 C₂₅H₂₁N₅O₈ 
• 38556-93-3 4-azido-benzoic acid ethyl ester 
• 149104-90-5 4-acetylphenylboronic acid 
• 459-57-4 4-fluorobenzaldehyde 
• 123-08-0 4-hydroxy-benzaldehyde 
• 18282-51-4 4-iodo-benzyl alcohol 
• 555-16-8 4-nitrobenzaldehdye 
• 23138-53-6 methyl 4-isocyanatobenzoate 
• 619-45-4 4-methoxycarbonyl aniline 
• 1015722-70-9 C₃₅H₃₆N₂O₁₃ 

Downstream Products

• 73771-52-5 (1Z,4E)-1,5-Bis-(4-azido-phenyl)-penta-1,4-dien-3-one 
• 206991-10-8 2-(4-azidophenyl)-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazol-3-oxide-1-oxyl 
• 1304513-31-2 C₁₉H₂₀N₄O₃ 
• 1304513-34-5 C₂₆H₂₃N₅O₇ 
• 1304513-35-6 C₂₆H₂₅N₅O₉ 
• 1304513-32-3 C₂₅H₂₁N₅O₈ 
• 1304513-41-4 C₄₆H₄₅N₅O₁₆ 

Relevant articles and documents

Influence of the substituent D/A at the 1,2,3-triazole ring on novel terpyridine derivatives: Synthesis and properties

In this study, we newly designed and developed a synthesis route based on the 1,3-dipolar cycloaddition of the derivatives of 4′-(1,2,3-triazol-4-yl)phenyl-2,2′:6′,2′′-terpyridine with various (hetero)aryl substituents, differing in electronic character, on a triazol ring. The obtained compounds were comprehensively characterized by UV-Vis spectroscopy and electrochemical and thermal studies. Moreover, preliminary biological tests were conducted. The investigation allowed the selection of materials with the most promising properties with particular emphasis on the nature of the substituents. In addition, theoretical studies (DFT and TD-DFT) were performed to verify the comprehensive understanding of experimental results.

One-pot synthesis of biopolymeric hollow nanospheres by photocrosslinking

Biopolymeric hollow nanospheres with stabilized structure have been prepared by self-assembly of amphiphatic photocrosslinkable carboxymethyl chitosans in a water medium into hollow nanocapsules and subsequent in situ photo-crosslinking of the photoreactive functional groups in the shells of the nanocapsules.

An examination of the utility of photogenerated reagents by using α chymotrypsin

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In vivo targeted delivery of antibodies into cancer cells with pH-responsive cell-penetrating poly(disulfide)s

Cell-penetrating poly(disulfide)s (CPDs) are promising vehicles for cytosolic delivery of proteins. However, currently available arginine-rich CPD has rarely been reported for systemic delivery due to its "always"positive charge. Herein, we developed pH-r

Photoredox-Catalyzed Four-Component Reaction for the Synthesis of Complex Secondary Amines

The one-pot sulfonylation/aminoalkylation of styrene derivatives furnishing substituted ?3-sulfonylamines was accomplished through a photoredox-catalyzed four-component reaction. Besides one molecule of water and the sodium counterion of the sulfinate, all atoms of the starting materials are transferred to the final product, rendering this process highly atom-efficient. The operationally simple protocol allows for the simultaneous formation of three new single bonds (C-S, C-N, and C-C) and therefore grants rapid access to structurally diverse products.