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[(3,4-dimethoxyphenyl)methyl](prop-2-en-1-yl)amine, also known as 3,4-dimethoxyphenylmethylprop-2-en-1-ylamine, is a chemical compound characterized by its molecular formula C14H19NO2. It is a tertiary amine with a substituted phenyl group and a prop-2-en-1-yl group attached to the amine nitrogen. [(3,4-dimethoxyphenyl)methyl](prop-2-en-1-yl)amine is recognized for its potential applications in the pharmaceutical and agrochemical industries, as well as its demonstrated biological activity, which makes it a significant subject of interest in medicinal chemistry research. Furthermore, it may also find use in the industrial synthesis of other organic compounds.

150970-55-1

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150970-55-1 Usage

Uses

Used in Pharmaceutical Synthesis:
[(3,4-dimethoxyphenyl)methyl](prop-2-en-1-yl)amine is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique chemical structure allows it to serve as a building block in the creation of complex molecules with potential therapeutic properties.
Used in Agrochemical Synthesis:
In the agrochemical industry, [(3,4-dimethoxyphenyl)methyl](prop-2-en-1-yl)amine is utilized as an intermediate for the development of compounds with pesticidal, herbicidal, or other agricultural applications. Its reactivity and structural features make it a valuable component in the design and synthesis of effective agrochemicals.
Used in Medicinal Chemistry Research:
[(3,4-dimethoxyphenyl)methyl](prop-2-en-1-yl)amine is also used as a subject of study in medicinal chemistry research. Its potential biological activity and unique structural features make it an interesting candidate for the development of new drugs and therapeutic agents. Researchers may explore its interactions with biological targets and its potential to modulate various biological pathways.
Used in Industrial Organic Synthesis:
[(3,4-dimethoxyphenyl)methyl](prop-2-en-1-yl)amine may have industrial applications as a chemical intermediate for the synthesis of other organic compounds. Its versatility in chemical reactions and its ability to be modified or functionalized make it a valuable component in the production of a wide range of organic chemicals for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 150970-55-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,9,7 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 150970-55:
(8*1)+(7*5)+(6*0)+(5*9)+(4*7)+(3*0)+(2*5)+(1*5)=131
131 % 10 = 1
So 150970-55-1 is a valid CAS Registry Number.

150970-55-1Downstream Products

150970-55-1Relevant academic research and scientific papers

Thiol-Ene Networks from Sequence-Defined Polyurethane Macromers

Alabi, Christopher A.,De Hoe, Guilhem X.,Hillmyer, Marc A.,Hoff, Emily A.,Mulvaney, Christopher M.

, p. 6729 - 6736 (2020)

To date, scalability limitations have hindered the exploration and application of sequence-defined polymers in areas such as synthetic plastics, fibers, rubbers, coatings, and composites. Additionally, the impact of sequence on the properties of cross-lin

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