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54752-27-1

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54752-27-1 Usage

General Description

2-(2-thienylidene)-1-tetralone is a chemical compound with the molecular formula C14H10OS. It is a yellowish powder with a molecular weight of 234.29 g/mol. 2-(2-THIENYLIDENE)-1-TETRALONE is a derivative of tetralone and contains a thienylidene group. It is used in the synthesis of various pharmaceuticals and organic compounds. It has potential applications in the development of new drugs and materials due to its unique chemical structure and properties. Additionally, it has been studied for its potential biological activities and pharmacological properties. Overall, 2-(2-thienylidene)-1-tetralone is a versatile chemical compound with potential applications in various fields including medicine, chemistry, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 54752-27-1 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, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54752-27:
(7*5)+(6*4)+(5*7)+(4*5)+(3*2)+(2*2)+(1*7)=131
131 % 10 = 1
So 54752-27-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H12OS/c16-15-12(10-13-5-3-9-17-13)8-7-11-4-1-2-6-14(11)15/h1-6,9-10H,7-8H2/b12-10+

54752-27-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(thiophen-2-ylmethylidene)-3,4-dihydronaphthalen-1-one

1.2 Other means of identification

Product number -
Other names -

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:54752-27-1 SDS

54752-27-1Relevant articles and documents

Selectivity in the Aerobic Dearomatization of Phenols: Total Synthesis of Dehydronornuciferine by Chemo- and Regioselective Oxidation

Esguerra, Kenneth Virgel N.,Lumb, Jean-Philip

supporting information, p. 1514 - 1518 (2018/01/27)

We describe a selective aerobic oxidation of meta-biaryl phenols that enables rapid access to functionalized phenanthrenes. Aerobic oxidations attract interest due to their efficiency, but remain underutilized in complex molecule settings due to challenge

Synthesis and Characterization of New Heterocyclic Compounds Containing Thienylbenzo[h]Quinoline Moiety

Al-Taifi, Elham A.,Abbady, Mohamed S.,Bakhite, Etify A.

, p. 1479 - 1487 (2016/09/24)

In this paper the reaction of 2-(2′-thienylmethylene)-3,4-dihydronaphthalen-2(1H)-one (1) with cyanothioacetamide gave a mixture of 3-cyano-5,6-dihydro-4-(2′-thienyl)-benzo[h]quinolin-2(1H)-thione (2) and the related disulfide 3. Compound 2 was reacted with some halo compounds namely; ethyl chloroacetate, chloroacetamide, chloro(N-(p-chlorophenyl))acetamide, N1-chloroacetylsulfanilamide, and 2-chloromethyl-1H-benzimidazole to produce a series of 2-(substituted)methylthio-3-cyano-5,6-dihydro-4-(2′-thienyl)benzo[h]quinolines 4a, 4b, 4c, 4d, 4e and 11. Upon heating the latter compounds with sodium ethoxide, they underwent intramolecular Thorpe–Zeigler cyclization to furnish the corresponding 2-(substituted)-3-amino-5,6-dihydro-4-(2′-thienyl)-benzo[h]thieno[2,3-b]quinolines 5a, 5b, 5c, 5d, 5e and 12. (3-Cyano-5,6-dihydro-4-(2′-thienyl)-benzo[h]quinolin-2-ylthio)acethydrazide (8) and the related isomer, 3-amino-5,6-dihydro-4-(2′-thienyl)thieno[2,3-b]benzo[h]quinoline-2-carbohydrazide (9), were also synthesized. Most of the aforementioned compounds were used as key intermediates for synthesizing other benzo[h]quinolines, benzo[h]thieno[2,3-b]quinolines as well as benzo[h]pyrimido[4′,5′:4,5] thieno[2,3-b]quinolines. The structure of all synthesized compounds was confirmed by spectroscopic measurements and analytical analyses.

Synthesis, spectral analysis, X-ray crystal structures and evaluation of chemical reactivity of five new benzoindazole derivatives through experimental and theoretical studies

Taib, Layla A.,Faidallah, Hassan M.,?ahin, Zarife Sibel,Asiri, Abdullah M.,?ahin, Onur,Arshad, Muhammad Nadeem

, p. 272 - 279 (2015/01/08)

The main purpose of this study was synthesis, X-ray, DFT and spectroscopic investigations of the title compounds (I-V). Five new compounds were synthesized and the detailed experimental results are reported. The crystal and molecular structures of the tit

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