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N,N'-di-p-tolyl-nonanediamide is a chemical compound with the molecular formula C21H30N2O2. It is a white crystalline solid that is soluble in organic solvents. N,N'-di-p-tolyl-nonanediamide is characterized by its two p-tolyl groups (each consisting of a methyl group attached to a phenyl ring) and a nonanediamide chain, which is a nine-carbon diamide chain. The compound is used in various applications, including as a chemical intermediate in the synthesis of pharmaceuticals and other organic compounds. It is also known for its potential use in the development of materials with specific properties, such as in polymer science. Due to its complex structure, it is important to handle N,N'-di-p-tolyl-nonanediamide with care, following proper safety protocols.

6876-58-0

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6876-58-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6876-58-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,7 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6876-58:
(6*6)+(5*8)+(4*7)+(3*6)+(2*5)+(1*8)=140
140 % 10 = 0
So 6876-58-0 is a valid CAS Registry Number.

6876-58-0Downstream Products

6876-58-0Relevant academic research and scientific papers

Synthesis of N,N′-diarylalkanediamides and their antimycobacterial and antialgal activity

Kubicova, Lenka,Waisser, Karel,Kunes, Jiri,Kralova, Katarina,Odlerova, Zelmira,Slosarek, Milan,Janota, Jiri,Svoboda, Zbynek

, p. 714 - 726 (2007/10/03)

A set of N,N′-diarylalkanediamides was synthesized. The compounds were tested for their antimycobacterial and antialgal activity. The antimycobacterial activity of N,N′-diarylalkanediamides depends on the lipophilicity of the respective acid. Antimycobacteri-ally active substances were found only in the series of N,N′-diarylethanediamides and N,N′-diarylbutanediamides. Other compounds (derivatives of pentane-, hexane-, octane- and nonanediamide) were inactive against various strains of mycobacteria. The compounds inhibited growth and chlorophyll production in Chlorella vulgaris. Their relatively low antial-gal activity is probably connected with their lowered aqueous solubility, and hence by a restricted passage of the inhibitor through the hydrophilic regions of thylakoid membranes.

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