6442-10-0 Usage
Description
DIETHYL-(3-METHYL-4-NITROSO)-ANILINE is a chemical compound characterized by its molecular formula C12H16N2O2. It presents as a yellow to brown crystalline solid, which is notable for its applications in various industrial processes.
Uses
Used in Dye and Pigment Production:
DIETHYL-(3-METHYL-4-NITROSO)-ANILINE is utilized as a key component in the production of dyes and pigments, contributing to the coloration and stability of these substances in various applications.
Used as a Reagent in Organic Synthesis:
In the field of organic chemistry, DIETHYL-(3-METHYL-4-NITROSO)-ANILINE serves as a reagent, facilitating specific chemical reactions and syntheses that are essential for creating a range of organic compounds.
Used as a Corrosion Inhibitor in Industrial Applications:
DIETHYL-(3-METHYL-4-NITROSO)-ANILINE also finds use as a corrosion inhibitor, helping to protect materials and structures from the damaging effects of corrosion in various industrial settings.
Safety and Precautions:
Given its toxic nature and potential carcinogenic properties, it is crucial to handle DIETHYL-(3-METHYL-4-NITROSO)-ANILINE with care and follow proper safety protocols. Adherence to regulations and guidelines for its safe storage and disposal is also of paramount importance to minimize risks to both human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 6442-10-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,4 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6442-10:
(6*6)+(5*4)+(4*4)+(3*2)+(2*1)+(1*0)=80
80 % 10 = 0
So 6442-10-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H16N2O/c1-4-13(5-2)10-6-7-11(12-14)9(3)8-10/h6-8H,4-5H2,1-3H3
6442-10-0Relevant articles and documents
Substituted 9-Diethylaminobenzo[ a]phenoxazin-5-ones (Nile Red Analogues): Synthesis and Photophysical Properties
Hornum, Mick,Mulberg, Mads W.,Szomek, Maria,Reinholdt, Peter,Brewer, Jonathan R.,Wüstner, Daniel,Kongsted, Jacob,Nielsen, Poul
supporting information, p. 1471 - 1488 (2021/01/13)
Nile Red is a benzo[a]phenoxazone dye containing a diethylamino substituent at the 9-position. In recent years, it has become a popular histological stain for cellular membranes and lipid droplets due to its unrivaled fluorescent properties in lipophilic environments. This makes it an attractive lead for chemical decoration to tweak its attributes and optimize it for more specialized microscopy techniques, e.g., fluorescence lifetime imaging or two-photon excited fluorescence microscopy, to which Nile Red has never been optimized. Herein, we present synthesis approaches to a series of monosubstituted Nile Red derivatives (9-diethylbenzo[a]phenoxazin-5-ones) starting from 1-naphthols or 1,3-naphthalenediols. The solvatochromic responsiveness of these fluorophores is reported with focus on how the substituents affect the absorption and emission spectra, luminosity, fluorescence lifetimes, and two-photon absorptivity. Several of the analogues emerge as strong candidates for reporting the polarity of their local environment. Specifically, the one- and two-photon excited fluorescence of Nile Red turns out to be very responsive to substitution, and the spectroscopic features can be finely tuned by judiciously introducing substituents of distinct electronic character at specific positions. This new toolkit of 9-diethylbenzo[a]phenoxazine-5-ones constitutes a step toward the next generation of optical molecular probes for advancing the understanding of lipid structures and cellular processes.
