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"Acetamide, N-(4-dodecyl-2-nitrophenyl)-" is a complex organic chemical compound with the molecular formula C18H27N2O3. It is a derivative of acetamide, where the hydrogen atom of the amide group is replaced by a 4-dodecyl-2-nitrophenyl group. Acetamide, N-(4-dodecyl-2-nitrophenyl)- is characterized by a long aliphatic chain (dodecyl) attached to a nitrophenyl ring, which is further connected to the acetamide moiety. It is used in various applications, such as in the synthesis of dyes and as an intermediate in the production of certain pharmaceuticals. Due to its specific structure, it may exhibit unique chemical and physical properties, making it a subject of interest in chemical research and industrial applications.

3663-31-8

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3663-31-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3663-31-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,6 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3663-31:
(6*3)+(5*6)+(4*6)+(3*3)+(2*3)+(1*1)=88
88 % 10 = 8
So 3663-31-8 is a valid CAS Registry Number.

3663-31-8Relevant academic research and scientific papers

Nouveaux diamino-3,4 phenylalcanes et leur transformation en benzimidazolemethanethiols-2

Krati, Noureddine,Roizard, Denis,Brembilla, Alain,Lochon, Pierre

, p. 443 - 448 (2007/10/02)

We report five o-phenylenediamines which are substituted by an aliphatic chain containing n carbon atoms (n = 4, 6, 8, 10, 12).We describe a well adapted general synthetic method using Schmidt's reaction.The diamines were then transformed into 2-benzimidazolemethanethiols and their related S-methyl derivatives which structures were checked by (1)H NMR.

4-higher alkyl-2-nitro-2'-hydroxy-3',5'-di-higher alkyl (or cumyl)-azobenzenes

-

, (2008/06/13)

4-Higher alkyl-2-nitro-2'-hydroxy-3',5'-di-higher alkyl (or cumyl)-azobenzenes are made by coupling the corresponding diazotized 4-higher alkyl-o-nitroaniline with the corresponding substituted phenol. These azobenzene intermediates are used to prepare the corresponding 2H-benzotriazole UV absorber stabilizers substituted on the 5-position of the benzo ring by a higher alkyl group, preferably tert-octyl or n-dodecyl.

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