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1-(4-chlorobenzyl)cyclopropanamine(SALTDATA: HCl) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27018-60-6

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27018-60-6 Usage

Uses

Used in Pharmaceutical Research and Development:
1-(4-chlorobenzyl)cyclopropanamine(SALTDATA: HCl) is used as a key intermediate in the synthesis of potential drug candidates for various medical conditions. Its unique chemical structure allows for the development of new therapeutic agents with improved efficacy and safety profiles.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(4-chlorobenzyl)cyclopropanamine(SALTDATA: HCl) serves as a valuable compound for exploring its pharmacological properties. Researchers can leverage its structural features to design and optimize new drugs targeting specific diseases or conditions.
Used in Drug Synthesis:
As a cyclopropanamine derivative with a chlorobenzyl group, 1-(4-chlorobenzyl)cyclopropanamine(SALTDATA: HCl) is used as a building block in the synthesis of various pharmaceutical compounds. Its incorporation into drug molecules can enhance their pharmacological activity and selectivity, leading to more effective treatments.
Used in Drug Design:

Check Digit Verification of cas no

The CAS Registry Mumber 27018-60-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,1 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27018-60:
(7*2)+(6*7)+(5*0)+(4*1)+(3*8)+(2*6)+(1*0)=96
96 % 10 = 6
So 27018-60-6 is a valid CAS Registry Number.

27018-60-6Relevant academic research and scientific papers

Synthesis of new cyclopropylisonitriles and their applications in Ugi four-component reactions

Osipova, Anna,Yufit, Dmitrii S.,De Meijere, Armin

, p. 131 - 139 (2008/01/03)

Several new cyclopropylisonitriles were synthesized from the corresponding cyclopropylamines (41-69% yield) and utilized in Ugi four-component reactions to furnish 12 new dipeptides in 38-86% yield. The structures of four of these dipeptides were determined by X-ray crystallography. Georg Thieme Verlag Stuttgart.

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