1-(3,4-Dichlorophenyl)-3-(4-phenoxyanilino)-1-propanone, commonly referred to as DAPP, is a chemical compound characterized by its molecular formula C18H15Cl2NO2. This ketone derivative features two aromatic rings, with one being phenyl and the other phenoxyanilino. DAPP is recognized for its utility in organic synthesis and medicinal chemistry, where it serves as a fundamental building block for the creation of diverse bioactive compounds and pharmaceutical drugs. Its structural attributes and chemical properties render DAPP a versatile and valuable molecule, not only in the development of novel drug candidates and agrochemicals but also in the realms of materials science and biotechnology.
477320-62-0
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Basic information
- Product Name: 1-(3,4-DICHLOROPHENYL)-3-(4-PHENOXYANILINO)-1-PROPANONE
- Synonyms: 1-(3,4-DICHLOROPHENYL)-3-(4-PHENOXYANILINO)-1-PROPANONE;SALOR-INT L233323-1EA
- CAS NO:477320-62-0
- Molecular Formula: C21H17Cl2NO2
- Molecular Weight: 386.27
- EINECS: N/A
- Product Categories: N/A
- Mol File: 477320-62-0.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 1-(3,4-DICHLOROPHENYL)-3-(4-PHENOXYANILINO)-1-PROPANONE(CAS DataBase Reference)
- NIST Chemistry Reference: 1-(3,4-DICHLOROPHENYL)-3-(4-PHENOXYANILINO)-1-PROPANONE(477320-62-0)
- EPA Substance Registry System: 1-(3,4-DICHLOROPHENYL)-3-(4-PHENOXYANILINO)-1-PROPANONE(477320-62-0)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 477320-62-0(Hazardous Substances Data)
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477320-62-0 Usage
Uses
Used in Organic Synthesis:DAPP is utilized as an intermediate in the synthesis of various organic compounds, leveraging its unique structure and reactivity to facilitate the formation of complex molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, DAPP is employed as a key component in the development of new pharmaceutical drugs, capitalizing on its chemical properties to enhance the therapeutic potential of these medications.
Used in the Development of Bioactive Compounds:
DAPP is used as a precursor in the creation of bioactive compounds, which possess the ability to interact with biological systems and may hold potential for various therapeutic applications.
Used in Agrochemicals:
DAPP is also utilized in the agrochemical industry, where it contributes to the development of new products designed to improve agricultural practices and crop protection.
Used in Materials Science:
Within the field of materials science, DAPP is explored for its potential applications in the development of novel materials with unique properties, such as enhanced stability or reactivity.
Used in Biotechnology:
In biotechnology, DAPP is investigated for its possible roles in the creation of new biological tools and systems, potentially contributing to advancements in areas such as drug discovery, genetic engineering, and bioprocessing.
Check Digit Verification of cas no
The CAS Registry Mumber 477320-62-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,7,3,2 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.Calculate Digit Verification of CAS Registry Number 477320-62:
(8*4)+(7*7)+(6*7)+(5*3)+(4*2)+(3*0)+(2*6)+(1*2)=160
160 % 10 = 0
So 477320-62-0 is a valid CAS Registry Number.
477320-62-0Upstream product
477320-62-0Downstream Products
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1-(3,4-DICHLOROPHENYL)-3-(4-PHENOXYANILINO)-1-PROPANONE
