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2-BROMO-2-PHENYLINDANE-1,3-DIONE is a chemical compound characterized by the molecular formula C16H9BrO2. It represents a brominated derivative of 2-phenylindane-1,3-dione, which is a substituted form of the parent compound 1,3-indandione. 2-BROMO-2-PHENYLINDANE-1,3-DIONE is distinguished by the presence of a bromine atom attached to the 2-phenyl ring, which endows it with unique chemical properties and reactivity. It plays a significant role in organic synthesis and pharmaceutical research, serving as a versatile building block for the creation of a variety of organic compounds.

1801-20-3

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1801-20-3 Usage

Uses

Used in Organic Synthesis:
2-BROMO-2-PHENYLINDANE-1,3-DIONE is utilized as a key intermediate in organic synthesis for the preparation of complex organic molecules. Its bromo-substituent allows for further functionalization and modification, making it a valuable precursor in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-BROMO-2-PHENYLINDANE-1,3-DIONE is employed as a building block for the development of new drugs. Its unique structure and reactivity contribute to the design and synthesis of novel therapeutic agents with potential applications in various medical fields.
Used in Agrochemical Development:
2-BROMO-2-PHENYLINDANE-1,3-DIONE also finds use in the agrochemical sector, where it serves as a starting material for the synthesis of new pesticides and other crop protection agents. Its chemical properties enable the development of innovative agrochemicals with improved efficacy and selectivity.
Used in Materials Science:
In the field of materials science, 2-BROMO-2-PHENYLINDANE-1,3-DIONE is explored for its potential applications in the synthesis of advanced materials with unique properties. Its structural features and reactivity can contribute to the development of new polymers, coatings, and other materials with specific characteristics for various applications.
Used in Academic Research:
2-BROMO-2-PHENYLINDANE-1,3-DIONE is important for academic research in organic chemistry, where it is studied for its reactivity, synthesis, and potential applications. It serves as a model compound for the development of new synthetic methodologies and the exploration of novel chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 1801-20-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,0 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1801-20:
(6*1)+(5*8)+(4*0)+(3*1)+(2*2)+(1*0)=53
53 % 10 = 3
So 1801-20-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H9BrO2/c16-15(10-6-2-1-3-7-10)13(17)11-8-4-5-9-12(11)14(15)18/h1-9H

1801-20-3SDS

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 2-bromo-2-phenylindene-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-Bromo-2-phenyl-1H-indene-1,3(2H)-dione

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:1801-20-3 SDS

1801-20-3Relevant academic research and scientific papers

Synthesis, characterization, antimicrobial activities and QSAR studies of some 10a-phenylbenzo[b]indeno[1,2-e][1,4]thiazin-11(10aH)-ones

Mor, Satbir,Pahal, Preeti,Narasimhan, Balasubramanian

, p. 176 - 189 (2012/07/31)

A series of 10a-phenylbenzo[b]indeno[1,2-e][1,4]thiazin-11(10aH)-ones (3) has been synthesized and tested for their antimicrobial activity. The antimicrobial evaluation data indicated that compounds, 3b, 3d, 3k and 3m exhibited very promising antibacterial activity and the compounds 3b and 3k exhibited notable activity, almost comparable to penicillin for Staphylococcus aureus and Bacillus subtilis respectively. The derivatives 3g and 3l exhibited high antifungal activity. Moreover, antibacterial activities were more prolific than antifungal activity. The QSAR studies indicated the importance of topological parameters, Kiers second order molecular index (κα 2) and molecular connectivity index (χ) in describing the antibacterial activity and electronic parameters, the energy of highest occupied molecular orbital (HOMO) and the dipole moment (μ) in describing the antifungal activity.

Synthesis and pharmacological properties of sulfur derivatives of indane-1,3-dione

Mitka, Katarzyna,Kowalski, Piotr,Sulko, Jerzy,Wozniak, Marian,Kloc, Jowita,Chodkowska, Anna,Jagiello-Wojtowicz, Ewa

, p. 387 - 393 (2007/10/03)

Synthesis of sulfur derivatives of indane-1,3-dione, VIIb-c, VIIIa-b, IX and X is described. Results of a preliminary pharmacological screening of six compounds [VIIb, VIII, VIIIb, IX, X and XI] are presented.

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