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Urea, N-(1,3-benzodioxol-5-ylmethyl)-N'-phenyl-, also known as 1-(3-phenylureido)propane-1,3-diyl bis(oxy-2,1-phenylene), is a chemical compound with the molecular formula C20H17N3O3. It is a white crystalline solid that is soluble in water and has a molecular weight of 351.37 g/mol. Urea, N-(1,3-benzodioxol-5-ylmethyl)-N'-phenyl- is a derivative of urea, featuring a phenyl group attached to the nitrogen atom and a 1,3-benzodioxol-5-ylmethyl group connected to the other nitrogen atom. It is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and other chemical compounds. Due to its unique structure, it exhibits specific properties that make it valuable in the development of new chemical entities with potential applications in various industries.

65609-33-8

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65609-33-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65609-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,0 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65609-33:
(7*6)+(6*5)+(5*6)+(4*0)+(3*9)+(2*3)+(1*3)=138
138 % 10 = 8
So 65609-33-8 is a valid CAS Registry Number.

65609-33-8Downstream Products

65609-33-8Relevant academic research and scientific papers

Self-Assembly of n-Alkyl- and Aryl-Side Chain Ureas and Their Derivatives as Evidenced by SEM and X-ray Analysis

Kulikov, Oleg V.,Siriwardane, Dumindika A.,McCandless, Gregory T.,Barnes, Charles,Sevryugina, Yulia V.,Desousa, Joseph D.,Wu, Jingbo,Sommer, Roger,Novak, Bruce M.

, p. 7511 - 7518 (2015)

A small library of ureas and related compounds was synthesized and examined by scanning electron microscopy (SEM), single-crystal X-ray diffraction, powder X-ray (pXRD), and polarized optical microscopy (POM) techniques in order to elucidate the factors controlling their self-assembly in the solid state. Inspection of the 12 solid-state structures revealed that molecules in the crystal lattice are held together by intermolecular H-bonding, π-π stacking as well as C-H/π interactions. The same interactions are likely responsible for the formation of supramolecular aggregates (e.g. sheet-like assemblies, micro- and nano-fibers, and the porous networks easily identifiable by SEM technique) and in certain cases led to the small molecules gelation.

Capsaicin-like analogue induced selective apoptosis in A2058 melanoma cells: Design, synthesis and molecular modeling

Pereira, Gustavo José Vasco,Tavares, Maurício Temotheo,Azevedo, Ricardo Alexandre,Martins, Barbara Behr,Cunha, Micael Rodrigues,Bhardwaj, Rajesh,Cury, Yara,Zambelli, Vanessa Olzon,Barbosa, Euzébio Guimar?es,Hediger, Matthias A.,Parise-Filho, Roberto

, p. 2893 - 2904 (2019/05/22)

The use of molecules inspired by natural scaffolds has proven to be a very promising and efficient method of drug discovery. In this work, capsaicin, a natural product from Capsicum peppers with antitumor properties, was used as a prototype to obtain urea

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