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5329-89-5

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5329-89-5 Usage

Description

1-(9,10-dihydrophenanthren-2-yl)ethanone, also known as 9,10-dihydroanthracen-2-yl methyl ketone, is an aromatic ketone compound characterized by a phenanthrene ring system and a ketone functional group. It is a yellow crystalline solid with a strong odor, and it exhibits sparing solubility in water but is soluble in organic solvents.

Uses

Used in Pharmaceutical Industry:
1-(9,10-dihydrophenanthren-2-yl)ethanone is used as a building block for the synthesis of various pharmaceuticals due to its unique chemical structure and properties, contributing to the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(9,10-dihydrophenanthren-2-yl)ethanone is utilized as a component in the synthesis of different agrochemicals, potentially enhancing crop protection and yield.
Used in Material Science:
1-(9,10-dihydrophenanthren-2-yl)ethanone is employed as a precursor in the creation of novel materials, leveraging its chemical properties to engineer advanced material solutions.
Used in Organic Synthesis:
As a key intermediate in organic synthesis, 1-(9,10-dihydrophenanthren-2-yl)ethanone is used to construct a wide array of organic compounds, serving as a versatile component in chemical reactions.
Used in Chemical Manufacturing:
In the field of chemical manufacturing, 1-(9,10-dihydrophenanthren-2-yl)ethanone is applied in the production process of various chemicals, playing a crucial role in the synthesis of specialty and fine chemicals.
Used in Biological and Pharmacological Research:
1-(9,10-dihydrophenanthren-2-yl)ethanone is studied for its potential biological and pharmacological activities, such as anti-inflammatory and antioxidant properties, which may lead to its use in therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5329-89-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,2 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5329-89:
(6*5)+(5*3)+(4*2)+(3*9)+(2*8)+(1*9)=105
105 % 10 = 5
So 5329-89-5 is a valid CAS Registry Number.

5329-89-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(9,10-dihydrophenanthren-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 2-acetyl-9,10-dihydrophenanthrene

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:5329-89-5 SDS

5329-89-5Relevant articles and documents

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Burger,Mosettig

, (1936)

-

LYSOPHOSPHATIDIC ACID RECEPTOR ANTAGONISTS

-

Paragraph 0585, (2013/03/26)

Compounds, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds to treat, prevent or diagnose diseases, disorders, or conditions associated with one or more of the lysophosphatidic acid receptors are provided.

Diene-yne cyclisation reactions of 1-ethynyl-2-vinyl-3,4- dihydronaphthalenes and 1-ethynyl-2-vinylnaphthalenes

Watanabe, Masataka,Shiine, Kodai,Ldeta, Keiko,Matsumoto, Taisuke,Thiemann, Thies

experimental part, p. 669 - 678 (2009/09/06)

The reaction of 1-ethynyl-2-vinyl-3,4-dihydronaphthalenes and 1-ethynyl-2-vinylnaphthalenes over RuCI2(p-cymene) PPh3 leads to 9,10-dihydrophenanthrenes and phenanthrenes in those cases where the ethynyl group in the substrates carries a terminal proton. When 1-phenylethynyl-2-vinyl-3,4-dihydronaphthalenes or 1-phenylethynyl-2- vinylnaphthalenes are reacted over Pt(PPh3)4, 1-methylene-1H-benz[e]-4,5-dihydroindenes and 1-methylene-1H-benz[e]indenes are formed.

RECHERCHES SUR LES SUBSTANCES MESOGENES-VIII; PREPARATION ET PROPERTIES MESOMORPHES DE SERIES ISOMETRIQUES

Malthete, Jacques,Canceill, Josette,Gabard, Jacqueline,Jacques, Jean

, p. 2815 - 2821 (2007/10/02)

The synthesis and the mesomorphic properties of various series of isometric mesogenic compounds are described.It is confirmed that isometric mesogenic molecules may be nematogenic and/or smectogenic according to the position of the polar rigid core.

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