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6833-23-4

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6833-23-4 Usage

Description

3-Methoxy-N-phenylbenzamide (CAS# 6833-23-4) is an organic compound characterized by its light pink solid appearance. It is primarily known for its utility in various organic synthesis processes, making it a valuable component in the field of chemistry.

Uses

Used in Organic Synthesis:
3-Methoxy-N-phenylbenzamide is used as a synthetic intermediate for the production of various organic compounds. Its unique chemical structure allows it to be a versatile building block in the synthesis of a wide range of molecules, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Methoxy-N-phenylbenzamide is used as a key component in the development of new drugs. Its incorporation into drug molecules can potentially enhance their therapeutic properties, such as improving their efficacy, selectivity, or bioavailability.
Used in Agrochemical Industry:
3-Methoxy-N-phenylbenzamide also finds application in the agrochemical industry, where it is utilized in the synthesis of novel pesticides, herbicides, and other crop protection agents. Its integration into these compounds can lead to the development of more effective and environmentally friendly products.
Used in Dye and Pigment Industry:
The light pink solid nature of 3-Methoxy-N-phenylbenzamide makes it a potential candidate for use in the dye and pigment industry. It can be employed in the creation of new colorants for various applications, such as textiles, plastics, and printing inks.
Used in Research and Development:
3-Methoxy-N-phenylbenzamide is also used in research and development settings, where it can serve as a model compound for studying various chemical reactions and mechanisms. Its unique properties make it an interesting subject for exploration in academic and industrial research labs.

Check Digit Verification of cas no

The CAS Registry Mumber 6833-23-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,3 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6833-23:
(6*6)+(5*8)+(4*3)+(3*3)+(2*2)+(1*3)=104
104 % 10 = 4
So 6833-23-4 is a valid CAS Registry Number.

6833-23-4SDS

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 3-Methoxy-N-phenylbenzamide

1.2 Other means of identification

Product number -
Other names 3-methoxy-benzoic acid 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:6833-23-4 SDS

6833-23-4Relevant articles and documents

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Hey,Long

, p. 4140,4113 (1959)

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Visible-Light Carbon Nitride-Catalyzed Aerobic Cyclization of Thiobenzanilides under Ambient Air Conditions

Bai, Jin,Yan, Sijia,Zhang, Zhuxia,Guo, Zhen,Zhou, Cong-Ying

supporting information, p. 4843 - 4848 (2021/06/28)

A metal-free heterogeneous photocatalysis has been developed for the synthesis of benzothiazoles via intramolecular C-H functionalization/C-S bond formation of thiobenzanilides by inexpensive graphitic carbon nitride (g-C3N4) under visible-light irradiation. This reaction provides access to a broad range of 2-substituted benzothiazoles in high yields under an air atmosphere at room temperature without addition of a strong base or organic oxidizing reagents. In addition, the catalyst was found to be stable and reusable after five reaction cycles.

Chromium-catalyzed ligand-free amidation of esters with anilines

Chen, Changpeng,Ling, Liang,Luo, Meiming,Zeng, Xiaoming

supporting information, p. 762 - 766 (2021/04/14)

Amides are important structural motifs in pharmaceutical and agrochemical chemistry because of the intriguing biological active properties. We report here the amidation of commercially available esters with anilines that was promoted by low-cost and air-stable chromium(III) pre-catalyst combined with magnesium, providing access to amides. This reaction occurs without the use of external ligands in a simple operation. Mechanistic studies indicate that a reactive aminated Cr species responsible for the amidation can be considered, which may be formed by reaction of low-valent Cr with aniline followed by reduction with hydrogen evolution.

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