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4-{(E)-[4-(dimethylamino)phenyl]diazenyl}benzoyl chloride is a complex organic chemical compound with the molecular formula C16H16ClN3O. It is characterized by a benzoyl chloride group attached to a benzene ring, which in turn is connected to a diazene group. The diazene group is linked to a 4-(dimethylamino)phenyl moiety, which contributes to the compound's reactivity and color. 4-{(E)-[4-(dimethylamino)phenyl]diazenyl}benzoyl chloride is often used as an intermediate in the synthesis of various dyes and pigments due to its ability to form stable azo compounds. Its chemical structure allows for a range of applications, including in the production of colored substances for industrial use.

27128-58-1

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27128-58-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27128-58-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,1,2 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 27128-58:
(7*2)+(6*7)+(5*1)+(4*2)+(3*8)+(2*5)+(1*8)=111
111 % 10 = 1
So 27128-58-1 is a valid CAS Registry Number.

27128-58-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[[4-(dimethylamino)phenyl]diazenyl]benzoyl chloride

1.2 Other means of identification

Product number -
Other names N,N-dimethyl-p-aminophenylazobenzoyl chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:27128-58-1 SDS

27128-58-1Upstream product

27128-58-1Relevant academic research and scientific papers

Polyfluorophore labels on DNA: Dramatic sequence dependence of quenching

Teo, Yin Nah,Wilson, James N.,Kool, Eric T.

supporting information; experimental part, p. 11551 - 11558 (2010/04/29)

We describe studies carried out in the DNA context to test how a common fluorescence quencher, dabcyl, interacts with oligodeoxynucleoside fluorophores (ODFs) - a system of stacked, electronically interacting fluorophores built on a DNA scaffold. We teste

Designing polymers for biphasic liquid/liquid separations after homogeneous reactions

Bergbreiter, David E.,Sung, Shayna D.,Li, Jun,Ortiz, Denisse,Hamilton, Patrick N.

, p. 461 - 468 (2013/09/05)

The phase-selective solubility properties of polymer supports that could be used in thermomorphic and latent biphasic systems useful in synthesis and catalysis were evaluated using polymers tagged with either visible dyes or fluorescent probes. Heptane/DMF, heptane/90% ethanol-water, heptane/ethyl acetate, heptane/ethanol, and heptane/tert-butyl alcohol solvent mixtures were all studied as examples of thermomorphic or latent biphasic systems. A range of polymers including polyisobutylene (PIB), poly(tert-butylstyrene) (PTBS), poly(octadecyl acrylate) (PODA), and poly(octadecyl methacrylate) (PODMA) were tested for hydrophobic phase-selective solubility. The results of these studies are compared to prior work with polar and nonpolar poly(N-alkylacrylamide)s and polystyrene. Together with this prior work, these results show that a wide range of polymers and solvent mixtures can be used for the recycling of soluble polymer-bound catalysts, reagents, and sequestrants using either thermomorphic or latent biphasic separation strategies.

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