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N,N'-1,2-ethanediylbis(4-methoxybenzamide) is a chemical compound with the molecular formula C18H20N2O5. It is an organic molecule that belongs to the class of amides, specifically a bisamide, which means it contains two amide groups connected by a linker. The compound is characterized by its two 4-methoxybenzamide groups, each featuring a methoxy substituent (-OCH3) on the para position of the benzene ring, and an amide group (-CO-NH2) attached to the benzene ring. The two benzamide groups are connected by a 1,2-ethanediyl (-CH2CH2-) linker, forming a symmetrical structure. N,N'-1,2-ethanediylbis(4-methoxybenzamide) is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its unique structure and properties.

3409-88-9

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3409-88-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3409-88-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,0 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3409-88:
(6*3)+(5*4)+(4*0)+(3*9)+(2*8)+(1*8)=89
89 % 10 = 9
So 3409-88-9 is a valid CAS Registry Number.

3409-88-9Relevant academic research and scientific papers

One-Pot Anodic Conversion of Symmetrical Bisamides of Ethylene Diamine to Unsymmetrical gem-Bisamides of Methylene Diamine

Golub, Tatiana,Dou, Gui-Yuan,Zeng, Cheng-Chu,Becker, James Y.

supporting information, p. 7961 - 7964 (2019/10/11)

Symmetrical bisamides of ethylene diamine of type ArCONHCH2CH2NHCOAr undergo anodic C-C bond cleavage in acetonitrile-LiClO4 under controlled-potential electrolysis. The electrogenerated carbocation intermediates react with the solvent acetonitrile to afford unsymmetrical gem-bisamides of type ArCONHCH2NHCOMe in a one-pot reaction. The yields of the latter products are moderate (up to 60%). Other minor products involve two symmetrical gem-bisamides of type ArCONHCH2NHCOAr and MeCONHCH2NHCOMe and fragmentation products (e.g., ArCONHCHO, ArCONH2, and ArCN).

Anodic oxidation of bisamides from diaminoalkanes by constant current electrolysis

Golub, Tatiana,Becker, James Y.

, p. 861 - 868 (2018/04/30)

In general, bisamides derived from diamines and involving 3 and 4 methylene groups as spacers between the two amide functionalities behave similar to monoamides upon anodic oxidation in methanol/LiClO4 because both types undergo majorly mono- and dimethoxylations at the α-position to the N atom. However, in cases where the spacer contains two methylene groups only the anodic process leads mostly to CH2-CH2 bond cleavage to afford products of type RCONHCH2OCH3. Moreover, upon replacing LiClO4 with Et4NBF4 an additional fragmentation type of product was generated from the latter amides, namely RCONHCHO. Also, the anodic process was found to be more efficient with C felt as the anode, and in a mixture of 1:1 methanol/acetonitrile co-solvents.

ANTIMICROBIAL COMPOUNDS

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Page/Page column 42, (2015/05/19)

The invention provides compounds for use in treating microbial infection in an animal. Example compounds include Pyridin-3-ylmethyl (4-((2-aminophenyl)- carbamoyl)benzyl)carbamate ("Entinostat"). The compounds can act via induction of the innate antimicrobial peptide defense system, and stimulation of autophagy.

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