N-Bromosuccinimide CAS# 128-08-5

BROMOSUCCINIMIDE-N, Promotion Season Now in Store and Free Sample for Testing with Factory Price

• Chemical Name:  N-Bromosuccinimide
• CAS No.:     128-08-5
• Molecular Fomula: ：C4H4BrNO2
• Molecular weight：177.98
• Appearance: white powder
• Sample：Available

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Description of BROMOSUCCINIMIDE-N

BROMOSUCCINIMIDE-N or NBS is a chemical reagent used in radical substitution and electrophilic addition reactions in organic chemistry. NBS can be a convenient source of Br•, the bromine radical.

Basic Info of BROMOSUCCINIMIDE-N

Basic Info
Numbering system
Properties
Basic Info

Numbering system

Properties

What is N-Bromosuccinimide?

• With the progress of science and technology and the development of society, chemical products have invariably permeated our daily lives, in medicine, food, cosmetics, electronics, industry, and other areas, becoming an essential part of our lives. One such product is N-Bromosuccinimide   which has developed particularly rapidly in recent years. Do you know about N-Bromosuccinimide  ?
• The official answer：N-bromosuccinimide, also known as N-bromosuccinimide, is an important brominating agent in organic synthesis, which has the advantages of mild reaction conditions, good selectivity, high yield, easy separation of products, etc. when bromination reaction. It is used in the free radical bromination reaction of allyl and benzyl; the electrophilic bromination reaction of ketone, aromatic compounds, or heterocyclic compounds and the addition reaction of olefins; and as catalyst and oxidant, etc. It is a common bromination reagent in the chemical and pharmaceutical industries.

What’s the application of N-Bromosuccinimide?

• As important intermediates of pharmaceuticals, pesticides, and organic polymer materials, bromosuccinimides are widely used and have a broad market prospect, and have an irreplaceable role in the chemical, pharmaceutical, and organic polymer materials industries. UsesN-bromosuccinimide reagents in organic reactions are traditionally used in allyl-position hydrogen, benzyl-position hydrogen, and brominated substitution of carbon-based α-position hydrogen. NBS can be produced by reacting an ice-cold NaOH solution of syringimide with equimolar bromine. It is mainly used in organic synthesis and rubber products additive is a special brominating agent for the preparation of allyl brominated olefins in the laboratory, and is also a reagent for the identification of primary, secondary, and tertiary alcohols. It is also used as a reagent to identify primary, secondary and tertiary alcohols. It can be used in the synthesis of bromoacetonitrile drugs, pesticide industry for the synthesis of thiamethoxam, as a fruit preservative, and organic synthesis materials such as antiseptic and anti-mildew agent, used to regulate low-energy bromination reactions, and also used in the production of rubber additives and pharmaceuticals. Can synthesize from acetonitrile medicine. The pesticide industry for the synthesis of thiamethoxam can also be used as fruit preservative and antiseptic, anti-mold agent, etc. It is also used as a reagent for the identification of primary, secondary, and tertiary alcohols and as an additive for rubber products, and as an important brominating agent in organic synthesis, and is often used as a brominating agent in the synthesis of antimicrobial agents in the pharmaceutical industry, such as the synthesis of benzyl cephalosporin (Cefaloram). Application Organic synthesis. Brominated olefins. Oxidation of ethanol to aldehydes and ketones. Oxidation of aldehydes to brominated acids. UsesMultifunctional brominating agent. Used for the oxidation of tryptophan, but tyrosine, histidine, and methionine residues may be oxidized to a lesser extent. Also used for modification of ribosomal sulfhydryl groups. General-purpose brominating agent. Oxidizes silyl ethers to aldehydes in the presence of AIBN. General-purpose bromination reagent; used for the oxidation of tryptophan, although tyrosine, histidine, and methionine oxidation residues may be present to a lesser extent; used for group modification of ribosomal sulfhydryl groups; oxidizes silyl ethers to aldehydes in the presence of AIBNand pharmaceutical industries.

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