4-(Allyloxy)-N,N,3,5-tetraethylbenzamide is a chemical compound characterized by the molecular formula C21H29NO2. It is a benzamide derivative featuring a tetraethyl substitution at the 3 and 5 positions and an allyloxy group at the 4 position. This white solid at room temperature is mainly utilized in research and experimentation within the realms of organic chemistry and pharmaceuticals.
7192-69-0
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Basic information
- Product Name: 4-(Allyloxy)-N,N,3,5-tetraethylbenzamide
- Synonyms: 4-(Allyloxy)-N,N,3,5-tetraethylbenzamide;N,N,3,5-tetraethyl-4-(2-propen-1-yloxy)benzamide
- CAS NO:7192-69-0
- Molecular Formula: C18H27NO2
- Molecular Weight: 289.4125
- EINECS: N/A
- Product Categories: N/A
- Mol File: 7192-69-0.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 432.7°Cat760mmHg
- Flash Point: 215.5°C
- Appearance: /
- Density: 0.979g/cm3
- Vapor Pressure: 1.09E-07mmHg at 25°C
- Refractive Index: 1.512
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 4-(Allyloxy)-N,N,3,5-tetraethylbenzamide(CAS DataBase Reference)
- NIST Chemistry Reference: 4-(Allyloxy)-N,N,3,5-tetraethylbenzamide(7192-69-0)
- EPA Substance Registry System: 4-(Allyloxy)-N,N,3,5-tetraethylbenzamide(7192-69-0)
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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: 7192-69-0(Hazardous Substances Data)
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7192-69-0 Usage
Uses
Used in Organic Chemistry Research:4-(Allyloxy)-N,N,3,5-tetraethylbenzamide is used as a research compound for exploring its chemical properties and potential interactions with other molecules, contributing to the advancement of organic chemistry.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 4-(Allyloxy)-N,N,3,5-tetraethylbenzamide is used as a precursor in the synthesis of new drugs, leveraging its unique structural features to develop novel therapeutic agents.
Used as a Building Block in Organic Synthesis:
4-(Allyloxy)-N,N,3,5-tetraethylbenzamide is employed as a building block in the synthesis of other organic compounds, potentially leading to the creation of new materials with specialized applications.
Check Digit Verification of cas no
The CAS Registry Mumber 7192-69-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,9 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.Calculate Digit Verification of CAS Registry Number 7192-69:
(6*7)+(5*1)+(4*9)+(3*2)+(2*6)+(1*9)=110
110 % 10 = 0
So 7192-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H27NO2/c1-6-11-21-17-14(7-2)12-16(13-15(17)8-3)18(20)19(9-4)10-5/h6,12-13H,1,7-11H2,2-5H3
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4-(Allyloxy)-N,N,3,5-tetraethylbenzamide
