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

54752-32-8

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54752-32-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54752-32-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,5 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54752-32:
(7*5)+(6*4)+(5*7)+(4*5)+(3*2)+(2*3)+(1*2)=128
128 % 10 = 8
So 54752-32-8 is a valid CAS Registry Number.

54752-32-8SDS

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 2-[(2-methylphenyl)methylidene]-3,4-dihydronaphthalen-1-one

1.2 Other means of identification

Product number -
Other names 2-(2-Methyl-benzyliden)-3,4-dihydro-2H-naphthalin-1-on

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:54752-32-8 SDS

54752-32-8Relevant academic research and scientific papers

Copper/GanPhos-Catalyzed 1,3-Dipolar Cycloaddition of Azo?-methine Ylides: An Efficient Access to Chiral Pyrrolidine Spirocycles

Gan, Zhenjie,Li, Ke,Zhang, Hui,Li, Er-Qing

supporting information, p. 1331 - 1340 (2020/11/30)

A highly efficient copper/GanPhos-catalyzed 1,3-dipolar cyclo?-addition?-of azomethine ylides is reported. This viable transformation provides a series of optically active spiro[dihydronaphthalene-2,3′-pyrrolidine]s, bearing one spiro quaternary and three tertiary stereogenic centers, in good yields and with high ee values. This protocol features high diastereo- A nd enantioselectivity, broad substrate scope and mild reaction conditions.

Radical C?N Borylation of Aromatic Amines Enabled by a Pyrylium Reagent

Chabbra, Sonia,Cornella, Josep,Leutzsch, Markus,Ma, Yuanhong,Niski, Jan,Pang, Yue,Reijerse, Edward J.,Schnegg, Alexander

supporting information, (2020/03/23)

Herein, we report a radical borylation of aromatic amines through a homolytic C(sp2)?N bond cleavage. This method capitalizes on a simple and mild activation via a pyrylium reagent (ScPyry-OTf) thus priming the amino group for reacti

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.

Manganese(I)-Catalyzed α-Alkenylation of Ketones Using Primary Alcohols

Gawali, Suhas Shahaji,Pandia, Biplab Keshari,Gunanathan, Chidambaram

supporting information, p. 3842 - 3847 (2019/05/24)

A simple protocol of manganese catalyzed selective α-alkenylation of ketones using primary alcohols is reported. The reactions proceeded well with a low loading of catalyst (0.3 mol %). The overall transformation operates through O-H bond activation of pr

Basic Anion-Exchange Resin-Catalyzed Aldol Condensation of Aromatic Ketones with Aldehydes in Continuous Flow

Laroche, Benjamin,Saito, Yuki,Ishitani, Haruro,Kobayashi, Shū

supporting information, p. 961 - 967 (2019/05/02)

A general method for the aldol condensation of aromatic ketones with aldehydes was developed under continuous-flow conditions using a commercially available, strongly basic anion-exchange resin (A26) as catalyst. This procedure, in addition to exhibiting a wide substrate scope, promoted carbon-carbon bond formation under mild conditions using a quasi-stoichiometric ratio of starting reagents with good to excellent yields, thereby forming a limited amount of waste and allowing the process to be applied to sequential-flow systems. A proof of concept was developed in the first fully heterogeneously catalyzed two-step flow synthesis of donepezil, which is a blockbuster commercial anti-Alzheimer's drug.

Discovery of 3,3a,4,5-tetrahydro-2H-benzo[g]indazole containing quinoxaline derivatives as novel EGFR/HER-2 dual inhibitors

Zong, Xi,Cai, Jin,Chen, Junqing,Sun, Chunlong,Li, Lushen,Ji, Min

, p. 24814 - 24823 (2015/03/30)

In the present study, twenty-five pyrazole-quinoxaline derivatives (4a-4y) were designed and synthesized, and their biological activity as potential EGFR or HER-2 kinase inhibitors was evaluated. Among them, compound 4l displayed better antiproliferative

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