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

3300-73-0

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3300-73-0 Usage

Chemical Class

Naphthalenone derivatives

Molecular Weight

260.72 g/mol

Pharmaceutical industry

Used in the production of various drugs and organic compounds.

Organic synthesis

Employed for the synthesis of other chemical compounds.

Biological Activities

Known to have potential biological activities, which can be utilized in the development of new drugs or compounds.

Precursor

Can be used as a precursor in the synthesis of other chemical compounds.

Aromatic Structure

Possesses an aromatic structure, which contributes to its chemical and biological properties.

Functional Groups

Contains functional groups that allow for various chemical reactions and interactions with other molecules.

Chemical and Biological Properties

Due to its aromatic structure and functional groups, it has the potential to exhibit a range of chemical and biological properties, making it a versatile compound in the fields of pharmaceuticals and organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 3300-73-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3300-73:
(6*3)+(5*3)+(4*0)+(3*0)+(2*7)+(1*3)=50
50 % 10 = 0
So 3300-73-0 is a valid CAS Registry Number.

3300-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorophenyl)-3,4-dihydro-2H-naphthalen-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:3300-73-0 SDS

3300-73-0Relevant academic research and scientific papers

Blue Light Promoted Difluoroalkylation of Aryl Ketones: Synthesis of Quaternary Alkyl Difluorides and Tetrasubstituted Monofluoroalkenes

Li, Kangkui,Chen, Jingchao,Yang, Chunhui,Zhang, Keyang,Pan, Chunxiang,Fan, Baomin,Fan, Baomin

supporting information, p. 4261 - 4265 (2020/06/04)

A facile and cost-effective method for the preparation of fluoroalkylated compounds has been described by the direct photoexcitation of halofluoroalkanes with blue light absorptivity, enabling the difluoroalkylation of aryl ketones. The methodology has provided an efficient, mild, and catalyst-free synthetic method for quaternary difluoroalkylated arenes and tetrasubstituted monofluoroalkenes.

A novel class of potential central nervous system agents. 3-Phenyl-2-(1-piperazinyl)-5H-1-benzazepines

Hino,Nagai,Uno,Masuda,Oka,Karasawa

, p. 107 - 117 (2007/10/02)

A series of 3-phenyl-2-piperazinyl-5H-1-benzazepines and related compounds were synthesized and evaluated for potential neuroleptic activity. The preparation of these compounds was carried out by 2,3-dichlorination of 3-phenyl-2,3,4,5-tetrahydro-1H-1-benz

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