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1(2H)-Naphthalenone, 3,4-dihydro-2-[(4-nitrophenyl)methylene]-, (2E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59082-21-2

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59082-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59082-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,8 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59082-21:
(7*5)+(6*9)+(5*0)+(4*8)+(3*2)+(2*2)+(1*1)=132
132 % 10 = 2
So 59082-21-2 is a valid CAS Registry Number.

59082-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-2-(4-nitrobenzylidene)-1-tetralone

1.2 Other means of identification

Product number -
Other names E-2-(4'-nitrobenzylidene)-1-tetralone

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:59082-21-2 SDS

59082-21-2Relevant academic research and scientific papers

A simple iron-catalyst for alkenylation of ketones using primary alcohols

Sk, Motahar,Kumar, Ashish,Das, Jagadish,Banerjee, Debasis

, (2020/04/10)

Herein, we developed a simple iron-catalyzed system for the α-alkenylation of ketones using primary alcohols. Such acceptor-less dehydrogenative coupling (ADC) of alcohols resulted in the synthesis of a series of important α,β-unsaturated functionalized ketones, having aryl, heteroaryl, alkyl, nitro, nitrile and trifluoro-methyl, as well as halogen moieties, with excellent yields and selectivity. Initial mechanistic studies, including deuterium labeling experiments, determination of rate and order of the reaction, and quantitative determination of H2 gas, were performed. The overall transformations produce water and dihydrogen as byproducts.

Synthesis of benzo[c]xanthones from 2-benzylidene-1-tetralones by the ultraviolet radiation-mediated tandem reaction

Xu, Wen-Zhi,Huang, Zhi-Tang,Zheng, Qi-Yu

, p. 5606 - 5608 (2008/12/21)

(Chemical Equation Presented) A facile one-pot method to prepare benzo[c]xanthones from readily accessible benzylidene-1-tetralones by the ultraviolet radiation-mediated tandem reaction is reported. The overall transformation presumably involves cis-trans

Solvent-free microwave enhanced synthesis of 2-arylidene-1-tetralones

Mogilaiah,Reddy, G. Randheer,Prashanthi

, p. 1535 - 1536 (2007/10/03)

A rapid and efficient method for the synthesis of 2-arylidene-1-tetralones 2 by the condensation of 1-tetralone 1 with aromatic aldehydes in the presence of p-toluenesulphonic acid (PTSA) in solvent free conditions under microwave irradiation is reported.

Ground- and excited-state properties of some 3,4-dihydro-1-(2-p-substituted benzylidene)naphthalenones: Substituent and environmental effects

Al-Ansari, Ibrahim A. Z.

, p. 687 - 696 (2007/10/03)

Electronic absorption and steady-state fluorescence emission of seven 3,4-dihydro-1-(2-p-substituted benzylidene)naphthalenones (1-7) show sizable solvent dependence. The charge-transfer (CT) absorption maxima of these compounds in various solvents show a

Synthesis of 3,3a-trans/cis-2-phenyl/acetyl-3-aryl-tetrahydroindeno/naphtho-and hexahydrobenzocycloheptapyrazoles as antiimplantation agents

Sinha, Anoop Kumar,Rastogi, Shri Nivas

, p. 684 - 692 (2007/10/02)

Reaction of benzocycloalkanones (1-3 and 24) and araldehydes (4-6) gives the arylideno-alkanones (7-12, 25 and 26) of which 11 and 12 on alkylation and acetylation afford alkyl ethers (13, 14 and 17) and acetates (15 and 16) respectively.Condensation of a

2-Substituted-1-naphthols as potent 5-lipoxygenase inhibitors with topical antiinflammatory activity

Batt,Maynard,Petraitis,Shaw,Galbraith,Harris

, p. 360 - 370 (2007/10/02)

The synthesis, biological evaluation, and structure-activity relationships of a series of 1-naphthols bearing carbon substituents at the 2-position are described. These compounds are potent inhibitors of the 5-lipoxygenase from RBL-1 cells and also inhibi

Heterocycles. Part VIII. Synthesis of New Substituted Benzindazoles

El-Rayyes, N. R.,Al-Jawhary, A.

, p. 135 - 140 (2007/10/02)

Aryl aldehydes I reacted with α-tetralone to give the corresponding 2-arylidene-1-tetralone II.Condensation of the latter chalcones with hydrazine, methylhydrazine and phenylhydrazine produced the corresponding benzoindazoles III, V and VI respectively

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