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  • N-[5-[[[5-[[3-(dimethylamino)propylamino]-oxomethyl]-1-methyl-3-pyrrolyl]amino]-oxomethyl]-1-methyl-3-pyrrolyl]-4-formamido-1-methyl-2-pyrrolecarboxamide

    Cas No: 2815-50-1

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  • 10 Milligram

  • Amadis Chemical Co., Ltd.
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2815-50-1 Usage

Description

5-Benzylsulfonyl-2-methoxy-aniline is a chemical compound characterized by the molecular formula C14H15NO3S. It is an aniline derivative featuring a benzene ring with a sulfonyl and a methoxy group attached. 5-Benzylsulfonyl-2-methoxy-aniline is known for its structural features and reactivity, making it a valuable component in the synthesis of organic compounds and pharmaceuticals. Its potential applications in medicinal chemistry and drug discovery are attributed to its ability to interact with enzymes and influence cellular processes, highlighting its significance in the fields of organic synthesis and pharmaceutical development.

Uses

Used in Organic Synthesis:
5-Benzylsulfonyl-2-methoxy-aniline is utilized as a key intermediate in the synthesis of various organic compounds. Its unique structural features and reactivity allow for the creation of a wide range of chemical products, contributing to the advancement of organic chemistry.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 5-Benzylsulfonyl-2-methoxy-aniline serves as a crucial building block for the development of new drugs. Its potential applications in medicinal chemistry are attributed to its ability to modulate biological activities, making it a promising candidate for the design and synthesis of novel therapeutic agents.
Used in Drug Discovery:
5-Benzylsulfonyl-2-methoxy-aniline is employed in drug discovery processes to identify and optimize potential drug candidates. Its structural features and reactivity enable the exploration of various chemical modifications, facilitating the discovery of new compounds with improved pharmacological properties.
Used in Enzyme Research:
5-Benzylsulfonyl-2-methoxy-aniline has been studied for its potential effects on enzymes, which is crucial for understanding its biological activities and potential therapeutic applications. By investigating its interactions with enzymes, researchers can gain insights into its mechanism of action and explore its potential use in the development of enzyme-targeting drugs.
Used in Cellular Process Studies:
5-Benzylsulfonyl-2-methoxy-aniline has also been examined for its impact on cellular processes, providing valuable information on its biological activities and potential applications in cell biology and medicine. Understanding its effects on cellular processes can aid in the development of targeted therapies and contribute to the advancement of cell-based treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 2815-50-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,1 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2815-50:
(6*2)+(5*8)+(4*1)+(3*5)+(2*5)+(1*0)=81
81 % 10 = 1
So 2815-50-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H15NO3S/c1-18-14-8-7-12(9-13(14)15)19(16,17)10-11-5-3-2-4-6-11/h2-9H,10,15H2,1H3

2815-50-1SDS

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 5-benzylsulfonyl-2-methoxyaniline

1.2 Other means of identification

Product number -
Other names 5-Benzylsulphonyl-o-anisidine

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:2815-50-1 SDS

2815-50-1Upstream product

2815-50-1Downstream Products

2815-50-1Relevant articles and documents

Metallized phenyl-azo-naphthol compounds

-

, (2008/06/13)

Metallized azo dyes of the formula STR1 wherein A is a sulfonyl, sulfonamido or carboxamido group, D is the residue of a phenol or naphthol, E is the residue of acetoacetanilide, a phenyl or naphthyl pyrazolone or the residue of a naphthol and M is a cation. The dyes are suitable for dyeing natural and synthetic polyamides, demonstrating good all-around fastness properties.

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