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1-(2-(2,4-Dichlorophenyl)-2-(geranyloxy)ethyl)-1H-imidazole is a complex chemical compound characterized by a 1H-imidazole core, with a 2-(geranyloxy)ethyl group and a 2,4-dichlorophenyl group attached to it. 1-(2-(2,4-Dichlorophenyl)-2-(geranyloxy)ethyl)-1H-imidazole is known for its potential applications in various fields due to its unique structural features.

135330-85-7

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135330-85-7 Usage

Uses

Used in Pharmaceutical Research and Development:
1-(2-(2,4-Dichlorophenyl)-2-(geranyloxy)ethyl)-1H-imidazole is used as a compound in pharmaceutical research and development for its potential to modulate cellular receptors or enzymes. Its unique structure makes it a candidate for drug discovery efforts, particularly in the development of new therapeutic agents.
Used in Agrochemical Research and Development:
In the agrochemical industry, 1-(2-(2,4-Dichlorophenyl)-2-(geranyloxy)ethyl)-1H-imidazole is used as a compound in research and development, with potential applications as a fungicide, pesticide, or antifungal agent. Its structural features suggest that it may have biological activity against various pests and pathogens, making it a valuable asset in the development of new agrochemical products.
Further studies are necessary to fully understand the potential uses and effects of 1-(2-(2,4-Dichlorophenyl)-2-(geranyloxy)ethyl)-1H-imidazole, as its complex structure and potential applications across different industries warrant a deeper investigation into its properties and capabilities.

Check Digit Verification of cas no

The CAS Registry Mumber 135330-85-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,3,3 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 135330-85:
(8*1)+(7*3)+(6*5)+(5*3)+(4*3)+(3*0)+(2*8)+(1*5)=107
107 % 10 = 7
So 135330-85-7 is a valid CAS Registry Number.
InChI:InChI=1/C21H26Cl2N2O/c1-16(2)5-4-6-17(3)9-12-26-21(14-25-11-10-24-15-25)19-8-7-18(22)13-20(19)23/h5,7-11,13,15,21H,4,6,12,14H2,1-3H3/b17-9+

135330-85-7Downstream Products

135330-85-7Relevant academic research and scientific papers

Structure-activity relationships of a new antifungal imidazole, AFK-108, and related compounds

Hori, Kimihiko,Sakaguchi, Akira,Kudoh, Michinari,Ishida, Koichi,Aoyama, Yuri,Yoshida, Yuzo

, p. 60 - 64 (2007/10/03)

Fungicidal activity of widely used imidazole antifungal drugs in topical applications is not so strong in spite of their potent fungistatic activities against dermatophytes and pathogenic yeasts. In order to improve fungicidal activity of imidazole antifungal agents, a series of novel imidazole derivatives having a hydrophobic substituent derived from isoprenoid were synthesized. The efficacy of these compounds was evaluated with respect to direct cell-membrane damaging activity, ergosterol biosynthesis inhibition, minimum growth-inhibitory concentration (MIC) and therapeutic effect for experimental dermatophytosis of guinea pigs. Among the newly synthesized compounds, the geranyl derivative named AFK-108 (2a) showed the highest in vivo fungicidal activity with both cell membrane damaging activity and ergosterol biosynthesis inhibition in vitro.

Azole derivatives and antifungal drugs containing the same as an active component

-

, (2008/06/13)

An azole derivative represented by the following formula (I): STR1 wherein X is a nitrogen atom or CH, Y is an oxygen atom, a sulfur atom, an imino group, a methylimino group or a group represented by =N O--, Z is one or two halogen atoms, in stands for a

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