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2-AMINO-3-BROMOBENZOPHENONE is a chemical compound characterized by the molecular formula C13H10BrNO. It is an aromatic ketone derivative that features a bromine atom and an amino group attached to a benzophenone core. 2-AMINO-3-BROMOBENZOPHENONE is recognized for its potential applications in medicinal chemistry, particularly due to its antimicrobial, antitumor activities, and its investigation as a photosensitizer in photodynamic therapy for cancer treatment.

808760-02-3

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808760-02-3 Usage

Uses

Used in Pharmaceutical Synthesis:
2-AMINO-3-BROMOBENZOPHENONE is utilized as an intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows it to be a key component in the creation of new drugs and molecules with therapeutic potential.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2-AMINO-3-BROMOBENZOPHENONE is studied for its potential biological and pharmacological properties. Its antimicrobial activity makes it a candidate for developing new antibiotics, while its antitumor properties suggest it could be used in the development of anticancer drugs.
Used in Photodynamic Therapy:
2-AMINO-3-BROMOBENZOPHENONE has been investigated for its potential as a photosensitizer in photodynamic therapy for cancer treatment. This application takes advantage of its ability to absorb light and generate reactive oxygen species, which can kill cancer cells upon light activation.
Used in Antimicrobial Applications:
2-AMINO-3-BROMOBENZOPHENONE is used as an antimicrobial agent for its ability to combat various microorganisms. This property is valuable in the development of new antibiotics to address the growing issue of antibiotic resistance.
Used in Antitumor Applications:
In the realm of oncology, 2-AMINO-3-BROMOBENZOPHENONE is used as an antitumor agent. Its potential to inhibit tumor growth and proliferation makes it a compound of interest for researchers working on novel cancer treatments.
Overall, 2-AMINO-3-BROMOBENZOPHENONE's diverse applications in different fields of study highlight its versatility and importance in the development of new therapeutic agents and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 808760-02-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,8,7,6 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 808760-02:
(8*8)+(7*0)+(6*8)+(5*7)+(4*6)+(3*0)+(2*0)+(1*2)=173
173 % 10 = 3
So 808760-02-3 is a valid CAS Registry Number.

808760-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-amino-3-bromophenyl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names 2-AMINO-3-BROMOBENZOPHENONE

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:808760-02-3 SDS

808760-02-3Relevant academic research and scientific papers

FUSED BICYCLIC COMPOUNDS USEFUL FOR MODULATING NUCLEIC ACID SPLICING

-

Page/Page column 179-180, (2021/09/04)

The present disclosure features compounds and related compositions that, inter alia, modulate nucleic acid splicing, e.g., splicing of a pre-mRNA, as well as methods of use thereof.

Mild and regioselective oxidative bromination of anilines using potassium bromide and sodium perborate

Roche, Didier,Prasad, Kapa,Repic, Oljan,Blacklock, Thomas J.

, p. 2083 - 2085 (2007/10/03)

The selective monobromination of various deactivated anilines using potassium bromide and sodium perborate as oxidant has been achieved. The use of ammonium molybdate as catalyst accelerates the rate of reaction but is not essential to obtain good yields and high selectivities. (C) 2000 Elsevier Science Ltd.

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