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3-Acetamido-1-bromo-2-nitrobenzene is a chemical compound that belongs to the class of aromatic nitro compounds. It is characterized by a benzene ring with an acetamido group at the 3 position, a bromo group at the 1 position, and a nitro group at the 2 position. 3-Acetamido-1-bromo-2-nitrobenzene is known for its potential applications in organic synthesis and pharmaceutical research, as well as its pharmacological properties such as anti-inflammatory and antimicrobial activity. However, it is important to handle 3-Acetamido-1-bromo-2-nitrobenzene with care due to its potential toxicity and hazardous properties.

99233-18-8

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99233-18-8 Usage

Uses

Used in Organic Synthesis:
3-Acetamido-1-bromo-2-nitrobenzene is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for the formation of different chemical bonds and reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In pharmaceutical research, 3-Acetamido-1-bromo-2-nitrobenzene is utilized as a starting material for the development of new drugs. Its potential pharmacological properties, such as anti-inflammatory and antimicrobial activity, make it a promising candidate for the treatment of various diseases and conditions. Researchers can modify its structure to explore its therapeutic potential and optimize its efficacy and safety.
Used in Medicinal Chemistry:
3-Acetamido-1-bromo-2-nitrobenzene is employed in medicinal chemistry for the design and synthesis of novel therapeutic agents. Its structural features can be exploited to create molecules with specific biological activities, targeting various diseases and disorders. 3-Acetamido-1-bromo-2-nitrobenzene can be a key component in the development of innovative drugs with improved pharmacokinetic and pharmacodynamic profiles.
Used in Chemical Research:
In chemical research, 3-Acetamido-1-bromo-2-nitrobenzene serves as a model compound for studying the reactivity and properties of aromatic nitro compounds. Its unique structure allows researchers to investigate various chemical reactions and mechanisms, contributing to the understanding of organic chemistry and the development of new synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 99233-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,2,3 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 99233-18:
(7*9)+(6*9)+(5*2)+(4*3)+(3*3)+(2*1)+(1*8)=158
158 % 10 = 8
So 99233-18-8 is a valid CAS Registry Number.

99233-18-8SDS

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 N-(3-Bromo-2-nitrophenyl)acetamide

1.2 Other means of identification

Product number -
Other names N-(3-bromo-2-nitrophenyl)acetamide

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:99233-18-8 SDS

99233-18-8Downstream Products

99233-18-8Relevant academic research and scientific papers

Regioselective ortho-nitration of N-phenyl carboxamides and primary anilines using bismuth nitrate/acetic anhydride

Lu, Yang,Li, Yaming,Zhang, Rong,Jin, Kun,Duan, Chunying

, p. 9422 - 9427 (2013)

An efficient and one-pot synthetic method for the regioselective ortho-nitration of the N-phenyl carboxamides and primary anilines has been developed by using bismuth nitrate and acetic anhydride as the nitrating reagents. Reaction proceeds at room temperature and results in corresponding ortho-nitrated products in moderate to excellent yields. This method provides an operationally simple, regioselective, and efficient access to synthesize o-nitro anilines under the mild conditions.

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