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52632-05-0

2-(P-DIMETHYLAMINOPHENYL)ETHYLAMINE

Catalog#: AR00DA7F  |   CAS#: 52632-05-0  |   MDL#: MFCD04114079  |   MF: C10H16N2  |   MW: 164.2474

Packsize Purity Price Availability Quantity
500mg 97% $180.00 Global Stock Buy Now Add To Cart
1g 97% $266.00 Global Stock Buy Now Add To Cart
5g 97% $786.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00DA7F
Chemical Name 2-(P-DIMETHYLAMINOPHENYL)ETHYLAMINE
CAS Number 52632-05-0
Molecular Formula C10H16N2
Molecular Weight 164.2474
MDL Number MFCD04114079
SMILES NCCc1ccc(cc1)N(C)C 

2-(4-Dimethylaminophenyl)ethylamine is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. As a substituted phenethylamine derivative, this compound serves as a valuable building block in the preparation of various organic molecules and pharmaceutical intermediates. Its primary application lies in its ability to introduce the 4-dimethylamino group into target molecules, thereby imparting distinct chemical characteristics and functional groups.In organic synthesis, 2-(4-Dimethylaminophenyl)ethylamine is frequently employed as a key starting material for the creation of complex molecular structures. By leveraging the amine functionality and the substituted phenyl ring, chemists can access a diverse array of chemical transformations, such as nucleophilic substitutions, reductive aminations, and condensation reactions. Additionally, the dimethylamino group can serve as a directing group in various synthetic strategies, enabling selective modifications and regioselective reactions.Furthermore, this compound plays a crucial role in the development of pharmaceutical compounds and bioactive molecules. The incorporation of the 4-dimethylaminophenyl moiety can significantly influence the biological activity, pharmacokinetics, and drug-receptor interactions of the final products. By leveraging the synthetic versatility of 2-(4-Dimethylaminophenyl)ethylamine, chemists can access a wide range of structurally diverse compounds with potential applications in drug discovery and medicinal chemistry.In summary, the application of 2-(4-Dimethylaminophenyl)ethylamine in chemical synthesis spans across various fields, including organic chemistry, pharmaceutical research, and material science. Its versatility and reactivity make it an indispensable tool for chemists seeking to access novel molecular architectures and functionalized compounds with tailored properties.
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GHS Pictogram
Signal Word Danger
UN# 2735
Hazard Statements H302+H312+H332-H314
Precautionary Statements P280-P305+P351+P338-P310
Class 8
Packing Group Ⅲ

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