6921-40-0

Basic information

• Product Name: 1-Azidonaphthalene
• Synonyms: 1-Azidonaphthalene;dicaesium 4,4'-methanediylbis(3-hydroxynaphthalene-2-carboxylate)
• CAS NO: 6921-40-0
• Molecular Formula: C₁₀H₇N₃
• Molecular Weight: 169.1827
• Mol File: 6921-40-0.mol
• Article Data: 64

Chemical Properties

• Melting Point: 12°C
• Boiling Point: 288.47°C (rough estimate)
• Flash Point: °C
• Appearance: /
• Density: 1.1713
• Refractive Index: 1.6550
• CAS DataBase Reference: 1-Azidonaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Azidonaphthalene(6921-40-0)
• EPA Substance Registry System: 1-Azidonaphthalene(6921-40-0)

Safety Data

• Hazardous Substances Data: 6921-40-0(Hazardous Substances Data)

Usage

Type of compound

Organic compound

Structure

Naphthalene ring with an azido group attached to the 1-position

Applications

a. Photoaffinity label
b. Photoremovable protecting group in organic chemistry

Photochemical property

Undergoes photochemical reactions upon exposure to ultraviolet light

Reaction outcome

Releases nitrogen gas

Utility

Valuable tool in biochemical and pharmaceutical research

Usage

Selectively label and modify biomolecules such as proteins and nucleic acids

Safety

Potentially hazardous compound

Precaution

Should be handled with care and proper safety measures

InChI:InChI=1/C10H7N3/c11-13-12-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H

Upstream product

• 134-32-7 1-amino-naphthalene 
• 91-20-3 naphthalene 
• 13922-41-3 1-Naphthylboronic acid 
• 86-57-7 1-Nitronaphthalene 
• 90-14-2 1-Iodonaphthalene 
• 39834-40-7 trans-2-bromo-1,2,3,4-tetrahydronaphthalen-1-ol 

Downstream Products

• 34774-85-1 1-amino-2-(methylthiomethyl)naphthalene 
• 134-32-7 1-amino-naphthalene 
• 91165-89-8 methyl 1-(1-naphthyl)-1,2,3-triazole-4-carboxylate 
• 110678-64-3 (1-(naphthalen-1-yl)-1H-1,2,3-triazole-4,5-diyl)bis(phenylmethanone) 
• 70292-12-5 5-methyl-1-(naphthalen-1-yl)-4-phenyl-1H-1,2,3-triazole 
• 2834-92-6 1-amino-2-naphthol 
• 487-10-5 1,2-di(naphthalen-1-yl)diazene 
• 7664-41-7 ammonia 
• 2243-55-2 1-(1-naphthyl)hydrazine 
• 861553-06-2 [1]naphthyl-triphenylphosphoranylidene-triazene 
• 40168-13-6 1-<(Triphenylphosphoranylidene)amino>naphthalene 
• 29005-25-2 1H-indene-2-carbonitrile 
• 29872-81-9 1H-indene-3-carbonitrile 
• 6141-93-1 (E)-di-[1]naphthyl-diazene 

Relevant articles and documents

A highly selective fluorescent sensor for mercury (II) ion based on Bodipy and Calix[4]arene bearing triazolenaphthylene groups; synthesis and photophysical investigations

A highly selective and sensitive fluorescent sensor for mercury ion has been obtained from a combination of Bodipy and Calix[4]arene derived by click chemistry. The structural characterization of all compounds had been carried out by FT-IR, 1H

The synthesis and crystal structure of 5-methyl-1-(1-naphthyl)-1,2,3- triazol-4-carboxyl acid

5-Methyl-1-(1-naphthyl)-1,2,3-triazol-4-carboxyl acid 3 was synthesized from 1-aminonaphthalene. The yielded product 3 was investigated with X-ray crystallographic, NMR, MS and IR techniques. Compound 3, C14H 11N3O2, Mr = 253.26, crystallizes in the orthorhombic space group Pbca with unit cell parameters a = 10.068(2), b = 12.353(2), c = 20.102(4) A, V = 2500.1(8) A3, Z = 8, Dx = 1.346 Mgm-3. The final R was 0.0474. The molecular packing is stabilized by intermolecular O-H???N interactions.

Design, synthesis and biological studies of some new imidazole-1,2,3-triazole hybrid derivatives

Some new 4-((1H-imidazol-1-yl)diarylmethyl)-5-methyl-1-aryl-1H-1,2,3-triazoles 7a-i were designed and synthesized by the one-pot reaction of diaryl-(1-aryl-5-methyl-1H-1,2,3-triazol-4-yl)methanol compounds with 1H-imidazole. The new compounds 7a-i were ch

Biocatalytic Aromaticity-Breaking Epoxidation of Naphthalene and Nucleophilic Ring-Opening Reactions

Aromatic hydroxylation reactions catalyzed by heme-thiolate enzymes proceed via an epoxide intermediate. These aromatic epoxides could be valuable building blocks for organic synthesis giving access to a range of chiral trans-disubstituted cyclohexadiene