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3-Ethoxy-4-methoxybenzaldehyde oxime is a chemical compound with the molecular formula C10H13NO2. It is an oxime derivative of benzaldehyde, featuring both ethoxy and methoxy groups on the benzene ring. This versatile compound is utilized in organic synthesis and pharmaceutical research as a reagent and intermediate, playing a crucial role in the preparation of pharmaceuticals, agricultural chemicals, and dyes. Moreover, it has been investigated for its potential biological activities, such as its anti-cancer properties and other therapeutic applications, making it a promising building block for the development of various functional molecules.

1956-36-1

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1956-36-1 Usage

Uses

Used in Pharmaceutical Research:
3-Ethoxy-4-methoxybenzaldehyde oxime is used as a reagent and intermediate in pharmaceutical research for its ability to contribute to the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Organic Synthesis:
In the field of organic synthesis, 3-Ethoxy-4-methoxybenzaldehyde oxime is employed as a key intermediate, facilitating the creation of a wide range of chemical compounds with diverse applications.
Used in Agricultural Chemicals:
3-Ethoxy-4-methoxybenzaldehyde oxime is used as a component in the development of agricultural chemicals, where its properties can be harnessed to enhance crop protection and yield.
Used in Dyes:
3-Ethoxy-4-methoxybenzaldehyde oxime is also utilized in the production of dyes, where its chemical structure contributes to the color and stability of the final product.
Used in Anticancer Applications:
3-Ethoxy-4-methoxybenzaldehyde oxime is studied for its potential as an anti-cancer agent, with research exploring its role in inhibiting cancer cell growth and its possible use in therapeutic interventions.
Used in Other Therapeutic Applications:
Beyond its anti-cancer potential, 3-Ethoxy-4-methoxybenzaldehyde oxime is also investigated for its possible applications in other therapeutic areas, highlighting its versatility and the broad scope of its potential impact on human health.

Check Digit Verification of cas no

The CAS Registry Mumber 1956-36-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,5 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1956-36:
(6*1)+(5*9)+(4*5)+(3*6)+(2*3)+(1*6)=101
101 % 10 = 1
So 1956-36-1 is a valid CAS Registry Number.

1956-36-1Relevant academic research and scientific papers

PYRIDO[2,3-D]PYRIMIDINE-2,4-DIAMINES AS PDE 2 INHIBITORS

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Page/Page column 28, (2010/02/12)

The invention provides compounds of formula (I) prodrugs thereof, and the pharmaceutically acceptable salts of the compounds or prodrugs, wherein n, X, and Y are as defined herein; pharmaceutical compositions thereof; combinations thereof; and uses thereo

Synthesis and Antitubercular Activity of 4-(5-Nitro-2-furyl/2-pyrazinyl/1-adamantyl)-2-(alkyl/aryl/arylamino)thiazoles

Khadse, B. G.,Lokhande, S. R.,Bhamaria, R. P.,Prabhu, S. R.

, p. 856 - 860 (2007/10/02)

The reaction of haloketones, obtained from Arndt-Eistert reaction on the acid chlorides of 1-adamantane, 5-nitrofuroic acid and pyrazine-2-carboxylic acid, with different thioamides and thioureas affords the title thiazoles (I-III).Some of them exhibit interesting antitubercular activity at 6.25 to 0.38 μg/ml concentration against H37Rv strain of M. tubercolosis in vitro testing.The structure activity relationship (SAR) has also been discussed.

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