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(2-(4-methoxyphenyl)cyclopropyl)methanamine is a cyclopropylamine derivative featuring a cyclopropyl ring attached to a phenyl group through a methoxy linker. This small molecule is distinguished by its unique structural features and potential biological activities, making it a promising candidate in medicinal chemistry and drug discovery.

1225705-84-9

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1225705-84-9 Usage

Uses

Used in Medicinal Chemistry:
(2-(4-methoxyphenyl)cyclopropyl)methanamine is utilized as a building block for the development of new drugs, capitalizing on its distinctive structure and the possibility of modulating various biological pathways.
Used in Drug Discovery:
As a chemical compound with potential therapeutic effects, (2-(4-methoxyphenyl)cyclopropyl)methanamine serves as a valuable starting point for the synthesis of novel bioactive molecules, contributing to the advancement of pharmaceutical research and innovation.

Check Digit Verification of cas no

The CAS Registry Mumber 1225705-84-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,5,7,0 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1225705-84:
(9*1)+(8*2)+(7*2)+(6*5)+(5*7)+(4*0)+(3*5)+(2*8)+(1*4)=139
139 % 10 = 9
So 1225705-84-9 is a valid CAS Registry Number.

1225705-84-9Relevant academic research and scientific papers

Lewis Basic Sulfide Catalyzed Electrophilic Bromocyclization of Cyclopropylmethyl Amide

Wong, Ying-Chieh,Ke, Zhihai,Yeung, Ying-Yeung

, p. 4944 - 4947 (2015/11/03)

A Lewis basic sulfide catalyzed electrophilic bromocyclization of cyclopropylmethyl amide has been developed. The catalytic protocol is applicable to both 1,1- and 1,2-substituted cyclopropylmethyl amides, giving oxazolines and oxazines in good yields and excellent diastereoselectivity.

A domino microwave-assisted protocol for the synthesis of 2,6-disubstituted pyrimidinones

Radi, Marco,Casaluce, Gianni,Botta, Maurizio

, p. 1997 - 2000 (2011/10/09)

A practical microwave-assisted protocol for the synthesis of 2,6-disubstituted pyrimidinones has been developed. This approach is based on a domino Michael addition-cyclocondensation reaction between substituted thioureas/guanidines and acetylenecarboxyla

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