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(1S)-1-(4-METHOXYPHENYL)PENTYLAMINE is a chemical compound with the molecular formula C14H21NO. It is an amine derivative that consists of a pentylamine chain with a 4-methoxyphenyl group attached to the first carbon. (1S)-1-(4-METHOXYPHENYL)PENTYLAMINE is commonly used in the field of pharmaceuticals and research as a building block for the synthesis of various drugs and bioactive molecules. Its unique chemical structure and biological properties make it a promising candidate for the development of new therapeutic agents. Additionally, (1S)-1-(4-METHOXYPHENYL)PENTYLAMINE may have interactions with certain biological targets, making it an area of interest for further investigation in drug discovery and medicinal chemistry.

848572-38-3

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848572-38-3 Usage

Uses

Used in Pharmaceutical Industry:
(1S)-1-(4-METHOXYPHENYL)PENTYLAMINE is used as a building block for the synthesis of various drugs and bioactive molecules. Its unique chemical structure and biological properties make it a valuable component in the development of new therapeutic agents.
Used in Research and Development:
(1S)-1-(4-METHOXYPHENYL)PENTYLAMINE is used as a research compound for investigating its interactions with certain biological targets. This helps in understanding its potential applications in drug discovery and medicinal chemistry, as well as in the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 848572-38-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,5,7 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 848572-38:
(8*8)+(7*4)+(6*8)+(5*5)+(4*7)+(3*2)+(2*3)+(1*8)=213
213 % 10 = 3
So 848572-38-3 is a valid CAS Registry Number.

848572-38-3Downstream Products

848572-38-3Relevant articles and documents

Preparation of Primary Amines and 2-Azetidinones via N-Trimethylsilyl Imines

Hart, David J.,Kanai, Ken-ichi,Thomas, Dudley G.,Yang, Teng-Kuei

, p. 289 - 294 (2007/10/02)

Nonenolizable aldehydes react with lithium bis(trimethylsilyl)amide at ambient temperatures to afford solutions of N-trimethylsilyl aldimines.Treatment of these solutions with Grignard reagents or alkyllithiums followed by an aqueous workup gives primary amines in moderate to excellent yields.Treatment of N-trimethylsilyl aldimines with ester enolates provides an expedient route to 1-unsubstituted 2-azetidinones.

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