150079-92-8

Basic information

• Product Name: 5-Bromo-2-chloro-N-ethylbenzamide
• Synonyms: 5-Bromo-2-chloro-N-ethylbenzamide;Ethyl 5-bromo-2-chlorobenzamide
• CAS NO: 150079-92-8
• Molecular Formula: C9H9BrClNO
• Molecular Weight: 262.53086
• Mol File: 150079-92-8.mol

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 5-Bromo-2-chloro-N-ethylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Bromo-2-chloro-N-ethylbenzamide(150079-92-8)
• EPA Substance Registry System: 5-Bromo-2-chloro-N-ethylbenzamide(150079-92-8)

Safety Data

• Hazardous Substances Data: 150079-92-8(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
5-Bromo-2-chloro-N-ethylbenzamide is used as an intermediate in the synthesis of new drugs for various therapeutic applications. Its unique structure allows for the development of innovative pharmaceuticals with potential benefits in treating a range of medical conditions.
Used in Agrochemical Industry:
In the agrochemical industry, 5-Bromo-2-chloro-N-ethylbenzamide serves as an intermediate in the preparation of various agrochemicals, contributing to the development of new pesticides and other agricultural products to enhance crop protection and yield.
Used in Chemical Research:
5-Bromo-2-chloro-N-ethylbenzamide is utilized in chemical research to study its biological activity and explore its potential applications in various fields. Its unique chemical properties make it an interesting subject for scientific investigation.
Used as a Reagent in Organic Reactions:
Due to its specific chemical structure and reactivity, 5-Bromo-2-chloro-N-ethylbenzamide is employed as a reagent in various organic reactions. It aids in the synthesis of complex organic compounds and contributes to the advancement of organic chemistry.

Upstream product

• 79-37-8 oxalyl dichloride 
• 21739-92-4 5-bromo-2-chlorobenzoic acid 
• 75-04-7 ethylamine 
• 188774-55-2 5-bromo-2-chlorobenzamide 

Relevant articles and documents

Efficient conversion of acids and esters to amides and transamidation of primary amides using OSU-6

OSU-6, an MCM-41 type hexagonal mesoporous silica with strong Bronsted acid properties, has been used to promote the high-yield conversion of carboxylic acids and esters to carboxamides as well as transamidations of primary amides in a one-pot solventless approach. A metal-free heterogeneous catalyst that promotes all of these processes has not been previously reported. OSU-6 enables these transformations to proceed in shorter times and at lower temperatures for a broad range of substrates. An added benefit is that the catalyst can be recycled and reused multiple times without significant loss of activity.

Fungicides for the control of take-all disease of plants

A method of controlling Take-All disease of plants by applying a fungicide of the formula STR1 wherein Z1 and Z2 are C and are part of an aromatic ring which is benzothiophene; and A is selected from --C(X)-amine wherein the amine is an unsubstituted, monosubstituted or disubstituted amino radical, --C(O)--SR3, --NH--C(X)R4, and --C(=NR3)--XR7 ; B is --Wm --Q(R2)3 or selected from O-tolyl, 1-naphthyl, 2-naphthyl, and 9-phenanthryl, each optionally substituted with halogen or R4 ; Q is C, Si, Ge, or Sn; W is --C(R3)p H(2-p) --; or when Q is C, W is selected from --C(R3)p H(2-p), --N(R3)m H(1-m)--, --S(O)p--, and --O--; X is 0 or S; n is 0, 1, 2, or 3; m is 0 or 1; p is 0, 1, or 2; each R and R2 is independently defined herein; R3 is C1 -C4 alkyl; R4 is C1 -C4 alkyl, haloalkyl, alkoxy, alkylthio, alkylamino, or dialkylamino; and R7 is C1 -C4 alkyl, haloalkyl, or phenyl, optionally substituted with halo, nitro, or R4 ; or an agronomic salt thereof.