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587-02-0

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587-02-0 Usage

Description

3-Ethylaniline, also known as 3-ethylaniline, is an organic compound with the chemical formula C8H11N. It is a clear brownish liquid that was analyzed in tobacco by mass-spectrometry method. 3-ETHYLANILINE is known for its role in the synthesis of various pharmaceutical agents and has potential applications in the field of drug development.

Uses

Used in Pharmaceutical Industry:
3-Ethylaniline is used as a reagent for the design, synthesis, and biological evaluation of thienopyrimidine hydroxamic acid-based derivatives. These derivatives serve as structurally novel histone deacetylase (HDAC) inhibitors, which are important in the development of treatments for various diseases, including cancer.
Additionally, 3-Ethylaniline is used in the synthesis and biological evaluation of novel 2-aminonicotinamide derivatives. These derivatives have potential applications as antifungal agents, contributing to the development of new treatments for fungal infections.

Check Digit Verification of cas no

The CAS Registry Mumber 587-02-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,8 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 587-02:
(5*5)+(4*8)+(3*7)+(2*0)+(1*2)=80
80 % 10 = 0
So 587-02-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H11N/c1-2-7-4-3-5-8(9)6-7/h3-6H,2,9H2,1H3

587-02-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Ethylaniline

1.2 Other means of identification

Product number -
Other names m-ethylaniline

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:587-02-0 SDS

587-02-0Relevant articles and documents

HZSM-5-Catalyzed Isomerization of Alkylanilines

Weigert, F. J.

, p. 3296 - 3298 (1987)

Zeolite HZSM-5 catalyzes the equilibration of toluidines and ethylanilines by an intramolecular 1,2-shift mechanism.The three xylidines with the 1,2,4-substitution pattern are also interconverted by this catalyst.Larger methylanilines are neither formed nor consumed by the catalyst.

Zeolite-Encaged Isolated Platinum Ions Enable Heterolytic Dihydrogen Activation and Selective Hydrogenations

Dai, Weili,Deng, Xin,Guan, Naijia,Li, Landong,Liu, Runze,Ma, Ding,Qin, Bin,Qin, Xuetao,Wu, Guangjun

supporting information, p. 20898 - 20906 (2021/12/14)

Understanding the unique behaviors of atomically dispersed catalysts and the origin thereof is a challenging topic. Herein, we demonstrate a facile strategy to encapsulate Ptδ+ species within Y zeolite and reveal the nature of selective hydrogenation over a Pt@Y model catalyst. The unique configuration of Pt@Y, namely atomically dispersed Ptδ+ stabilized by the surrounding oxygen atoms of six-membered rings shared by sodalite cages and supercages, enables the exclusive heterolytic activation of dihydrogen over Ptδ+···O2- units, resembling the well-known classical Lewis pairs. The charged hydrogen species, i.e., H+ and Hδ-, are active reagents for selective hydrogenations, and therefore, the Pt@Y catalyst exhibits remarkable performance in the selective hydrogenation of α,β-unsaturated aldehydes to unsaturated alcohols and of nitroarenes to arylamines.

Highly selective hydrogenation of aromatic ketones to alcohols in water: effect of PdO and ZrO2

Alsalahi, W.,Trzeciak, A. M.,Tylus, W.

, p. 10386 - 10393 (2021/08/09)

Pd/ZrO2and PdO/ZrO2composites, containing Pd or PdO nanoparticles, were prepared using an original one-step methodology. These nanocomposites catalyze the hydrogenation of acetophenone (AP) at 1 bar and 10 bar of H2in an aqueous solution. Compared to unsupported Pd or PdO nanoparticles, a remarkable increase in their activity was achieved as a result of interaction with zirconia. An unsupported PdO hydrogenated AP mainly to ethylbenzene (EB), while excellent regioselectivity towards 1-phenylethanol (PE) was obtained with PdO/ZrO2and it was preserved during recycling. Similarly, regioselectivity to PE was higher with Pd/ZrO2compared to unsupported Pd NPs. PdO and zirconia resulted in high selectivity to alcohols in the hydrogenation of substituted acetophenones.

Pd-Nanoparticles immobilized organo-functionalized SBA-15: An efficient heterogeneous catalyst for selective hydrogenation of C–C double bonds of α,β-unsaturated carbonyl compounds

Burri, David Raju,Narani, Anand,Natte, Kishore,Reddy Kannapu, Hari Prasad

, (2020/10/05)

A novel PdNPs/SBA-NH2-LA catalyst has been prepared by a post-synthetic grafting approach via successive anchoring of propylamine (SBA-NH2) and lipoic acid (SBA-NH2-LA) functional groups followed by palladium nanoparticles immobilization. The Physico-chemical properties of the catalyst were extensively investigated by XRD, N2 adsorption-desorption, XPS, FT-IR, and TEM analysis. The PdNPs/SBA-NH2-LA catalyst is found to be highly selective for the hydrogenation of C–C double bonds of α, β-unsaturated carbonyl compounds. Excellent conversion (95–99 %) and selectivity (>99 %) with high turn over frequency (330?1065 h?1) achieved at room temperature under atmospheric hydrogen pressure within 30?90 min of reaction time. This kind of high activity is expected from its structural and textural integrity of the catalyst.

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