100-04-9

Basic information

• Product Name: 4-(N,N-dimethylamino)benzenediazonium chloride
• Synonyms: 4-(N,N-dimethylamino)benzenediazonium chloride;DIAZONIUMCHLORIDE;4-N,N-DIMETHYLAMINOBENZENE;4-(dimethylamino)benzenediazonium:chloride
• CAS NO: 100-04-9
• Molecular Formula: C₈H₁₀N₃*Cl
• Molecular Weight: 183.6381
• EINECS: 202-813-8
• Mol File: 100-04-9.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(N,N-dimethylamino)benzenediazonium chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(N,N-dimethylamino)benzenediazonium chloride(100-04-9)
• EPA Substance Registry System: 4-(N,N-dimethylamino)benzenediazonium chloride(100-04-9)

Safety Data

• Hazardous Substances Data: 100-04-9(Hazardous Substances Data)

Usage

Contact allergens

It is a diazo compound found in diazo copy paper. It is allergenic only when unexposed.

InChI:InChI=1/C8H10N3.B.4FH/c1-11(2)8-5-3-7(10-9)4-6-8;;;;;/h3-6H,1-2H3;;4*1H/q+1;+3;;;;/p-4

Upstream product

• 536-46-9 4-dimethylaminophenylamine dihydrochloride 
• 110-46-3 isopentyl nitrite 
• 99-98-9 4-amino-N,N-dimethylaniline 
• 536-47-0 N,N-dimethyl-1,4-phenylenediamine sulfate 

Downstream Products

• 93872-93-6 4-(azulen-1-yl-trans-azo)-N,N-dimethyl-aniline 
• 54417-83-3 (4-N,N-dimethyl-aminophenyl)-(4N-methyl-pyridinio)-acetylene iodide 
• 3150-84-3 N,N-dimethyl-4-(2-chloro-4-nitrophenylazo)aniline 
• 21420-49-5 1-(p-dimethylaminophenyl)-3,5-diphenylformazan 
• 108124-90-9 N,N-dimethyl-4-(2-methyl-4-nitro-phenylazo)-aniline 
• 619-60-3 4-(N,N-dimethylamino)phenol 
• 99-98-9 4-amino-N,N-dimethylaniline 
• 18523-44-9 p-(dimethylamino)phenyl azide 

Relevant articles and documents

Parallel synthesis of "Click" chalcones as antitubulin agents

It has been shown that some chalcones are able to inhibit tubulin polymerization, giving cytotoxicity and destruction of tumoral vasculature. A library of 180 novel chalcone analogs has been synthesized via click chemistry and screened for their cytotoxic

Surface Functionalisation Using Arylcarbene Reactive Intermediates

A process for producing a substrate having a functionalised surface, which process comprises contacting the substrate with a carbene precursor, which carbene precursor is a compound of formula (III) or (IV) whose substituent groups are defined herein: (b)

Substituent Effects on 13C and 15N Chemical Shifts in Triazenes Studied by Principal Components Multivariate Data Analysis

Principal components analysis was applied to the 13C and 15N chemical shift data on a series of fifteen 1-(para-substituted-phenyl)-3-acetyl-3-methyltriazenes.It was found that the halogen-substituted triazenes formed a class, based on substituent effects, which was different from the remaining eleven triazenes.A one-component model described the halogen class, whereas a two-component model was necessary for a description of the second class.In the second class, substituent tended to cluster to form groups depending on their electronic character.

TETRAZOLE DERIVATIVES. 26. 2-ARYL-3-(p-DIMETHYLAMINOPHENYL)-5-PHENYLTETRAZOLIUM

Deeply colored tetrazolium salts were obtained by oxidation of triarylformazans containing a p-dimethylamino group in the N-phenyl substituent with bromine or nitrous acid.