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(Z)-1-(3-bromoprop-1-enyl)-4-methoxybenzene is a chemical compound characterized by its molecular formula C10H11BrO. It features a benzene ring with a methoxy group (CH3O-) and a bromine-substituted propenyl group (-CH=CH-CH2Br) attached to it. This unique structure endows the compound with potential applications in various fields, particularly pharmaceuticals and agrochemicals. Due to its chemical nature, it is crucial to handle (Z)-1-(3-bromoprop-1-enyl)-4-methoxybenzene with caution, as it may possess hazardous properties and should be utilized by trained professionals in a controlled environment.

1374587-86-6

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1374587-86-6 Usage

Uses

Used in Pharmaceutical Industry:
(Z)-1-(3-bromoprop-1-enyl)-4-methoxybenzene is used as an intermediate compound for the synthesis of various pharmaceutical products. Its unique structure allows it to be a key component in the development of new drugs, potentially contributing to the treatment of different medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, (Z)-1-(3-bromoprop-1-enyl)-4-methoxybenzene is utilized as a building block for the creation of novel agrochemicals. Its properties make it a valuable asset in the development of pesticides, herbicides, and other agricultural chemicals that can enhance crop protection and yield.

Check Digit Verification of cas no

The CAS Registry Mumber 1374587-86-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,5,8 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1374587-86:
(9*1)+(8*3)+(7*7)+(6*4)+(5*5)+(4*8)+(3*7)+(2*8)+(1*6)=206
206 % 10 = 6
So 1374587-86-6 is a valid CAS Registry Number.

1374587-86-6Relevant academic research and scientific papers

Synthesis, Biological Activity, and ADME Properties of Novel S-DABOs/N-DABOs as HIV Reverse Transcriptase Inhibitors

Radi, Marco,Pagano, Mafalda,Franchi, Luigi,Castagnolo, Daniele,Schenone, Silvia,Casaluce, Gianni,Zamperini, Claudio,Dreassi, Elena,Maga, Giovanni,Samuele, Alberta,Gonzalo, Encarna,Clotet, Bonaventura,Este, Jose A.,Botta, Maurizio

experimental part, p. 883 - 896 (2012/08/08)

Previous studies aimed at exploring the SAR of C2-functionalized S-DABOs demonstrated that the substituent at this position plays a key role in the inhibition of both wild-type RT and drug-resistant enzymes, particularly the K103N mutant form. The introdu

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