Welcome to LookChem.com Sign In|Join Free

CAS

  • or

10286-76-7

Post Buying Request

10286-76-7 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

10286-76-7 Usage

Description

N1-(2,4-Dichlorophenyl)benzamide, a chemical compound with the molecular formula C13H9Cl2NO, is a benzamide derivative characterized by the presence of two chlorine atoms attached to a phenyl ring. N1-(2,4-DICHLOROPHENYL)BENZAMIDE holds potential in the pharmaceutical and organic synthesis industries, serving as a building block for the creation of biologically active molecules and pharmaceutical drugs. Its unique structure and properties make it a subject of interest for further research into its possible pharmacological activities.

Uses

Used in Pharmaceutical Industry:
N1-(2,4-Dichlorophenyl)benzamide is used as a building block for the synthesis of various biologically active molecules and pharmaceutical drugs. Its unique structure allows for the development of new compounds with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, N1-(2,4-Dichlorophenyl)benzamide serves as a key intermediate for the production of a range of chemical compounds. Its versatility in chemical reactions makes it a valuable component in the synthesis of various organic compounds.
Used in Research and Development:
N1-(2,4-Dichlorophenyl)benzamide is used as a subject of research for its potential pharmacological activities. Its biological effects and interactions with biological systems are of interest to scientists, who aim to explore its possible applications in medicine and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 10286-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,8 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10286-76:
(7*1)+(6*0)+(5*2)+(4*8)+(3*6)+(2*7)+(1*6)=87
87 % 10 = 7
So 10286-76-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H9Cl2NO/c14-10-6-7-12(11(15)8-10)16-13(17)9-4-2-1-3-5-9/h1-8H,(H,16,17)

10286-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,4-dichlorophenyl)benzamide

1.2 Other means of identification

Product number -
Other names benzoic acid-(2,4-dichloro-anilide)

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:10286-76-7 SDS

10286-76-7Relevant articles and documents

Copper-catalyzed synthesis of arylcarboxamides from aldehydes and isocyanides: The isocyano group as an N1 synthon

Liu, Jian-Quan,Shen, Xuanyu,Liu, Zhenhua,Wang, Xiang-Shan

, p. 6314 - 6317 (2017)

An interesting radical coupling reaction of aromatic aldehydes with isocyanides was disclosed for the synthesis of amides catalyzed by copper. According to the experimental results and mechanistic study, the isocyano group acted as an N1 synthon rather than exhibiting the carbene-like reactivity, exploiting a new reactivity profile of isocyanides.

Efficient Electrocatalysis for the Preparation of (Hetero)aryl Chlorides and Vinyl Chloride with 1,2-Dichloroethane

Liang, Yujie,Lin, Fengguirong,Adeli, Yeerlan,Jin, Rui,Jiao, Ning

supporting information, p. 4566 - 4570 (2019/02/14)

Although the application of 1,2-dichloroethane (DCE) as a chlorinating reagent in organic synthesis with the concomitant release of vinyl chloride as a useful byproduct is a fantastic idea, it still presents a tremendous challenge and has not yet been achieved because of the harsh dehydrochlorination conditions and the sluggish C?H chlorination process. Here we report a bifunctional electrocatalysis strategy for the catalytic dehydrochlorination of DCE at the cathode simultaneously with anodic oxidative aromatic chlorination using the released HCl as the chloride source for the efficient synthesis of value-added (hetero)aryl chlorides. The mildness and practicality of the protocol was further demonstrated by the efficient late-stage chlorination of bioactive molecules.

Amide-assisted radical strategy: Metal-free direct fluorination of arenes in aqueous media

Liang, Deqiang,Li, Yanni,Gao, Shulin,Li, Renlun,Li, Xiangguang,Wang, Baoling,Yang, Hai

supporting information, p. 3344 - 3349 (2017/07/28)

A metal- and initiator-free direct fluorination of arenes with the assistance of an amide group is developed. This reaction proceeded under simple aqueous conditions with good functional group tolerance and ortho-para selectivity, and is highly practical because it could be readily scaled up to a multigram-scale. At this stage, an exclusive mechanism could not be proposed, and several possibilities have been discussed. The possibility of the amide-assisted radical chain mechanism has been supported by experimental and computational investigations as well as a seminal work.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 10286-76-7