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Acetamide, N-(4-morpholinylphenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37733-80-5

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37733-80-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37733-80-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,3 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 37733-80:
(7*3)+(6*7)+(5*7)+(4*3)+(3*3)+(2*8)+(1*0)=135
135 % 10 = 5
So 37733-80-5 is a valid CAS Registry Number.

37733-80-5Downstream Products

37733-80-5Relevant academic research and scientific papers

Synthesis, characterization and antimicrobial studies of a new mannich base N-[morpholino (phenyl)methyl]acetamide and Its cobalt(II), nickel(II) and copper(II) metal complexes

Muruganandam,Krishnakumar

, p. 875 - 882 (2012)

A new Mannich base N-[morpholino(phenyl)methyl]acetamide (MBA), was synthesized and characterized by spectral studies. Chelates of MBA with cobalt(II), nickel(II) and copper(II) ions were prepared and characterized by elemental analyses, IR and UV spectral studies. MBA was found to act as a bidentate lig and , bonding through the carbonyl oxygen of acetamide group and CNC nitrogen of morpholine moiety in all the complexes. Based on the magnetic moment values and UV-Visible spectral data, tetracoordinate geometry for nitrato complexes and hexacoordinate geometry for sulphato complexes were assigned. The antimicrobial studies show that the Co(II) nitrato complex is more active than the other complexes.

Peroxo complexes of uranium(VI) containing nitrogen and oxygen donor ligands1

Singh, Balgar,Mahajan, Simpy,Sheikh,Sharma, Mohita,Kalsotra, Bansi Lal

body text, p. 1079 - 1088 (2012/10/08)

The uranium(VI) peroxo complexes containing Mannich base ligands having composition [UO(O2)L-L(NO3)2] {where L-L = morpholinobenzyl acetamide (MBA), piperidinobenzyl acetamide (PBA), morpholinobenzyl benzamide (MBB), piper

Solvent-free synthesis of monoacylaminals from the reaction of amides and aminals as precursors in carbinolamide synthesis

Sansone, Matthew F.,Koyanagi, Takaoki,Przybyla, David E.,Nagorski, Richard W.

supporting information; experimental part, p. 6031 - 6033 (2010/11/21)

A solvent-free method of generating monoacylaminals by heating the amide and aminal starting materials in the presence of one another has been developed. Yields were generally between 45% and 65% with the monoacylaminal being isolated, needing no further purification after drying under high vacuum.

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