5469-91-0 Usage
Description
(2E)-2-[4-(dimethylamino)phenyl]imino-1-phenylethanone is a bright yellow solid with a molecular formula C17H17N3O. It is a compound that contains a phenyl group, a dimethylamino group, and an imine functional group. (2E)-2-[4-(dimethylamino)phenyl]imino-1-phenylethanone is commonly used in organic synthesis and pharmaceutical research due to its structural and chemical properties.
Uses
Used in Pharmaceutical Research:
(2E)-2-[4-(dimethylamino)phenyl]imino-1-phenylethanone is used as a compound in pharmaceutical research for its potential applications in the development of drugs or pharmaceuticals. Its unique structure and chemical properties make it a promising candidate for further exploration and research.
Used in Organic Synthesis:
(2E)-2-[4-(dimethylamino)phenyl]imino-1-phenylethanone is used as a reagent in organic synthesis, where it can be utilized to create a variety of other compounds. Its versatility and unique functional groups make it a valuable component in the synthesis of various organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 5469-91-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5469-91:
(6*5)+(5*4)+(4*6)+(3*9)+(2*9)+(1*1)=120
120 % 10 = 0
So 5469-91-0 is a valid CAS Registry Number.
5469-91-0Relevant articles and documents
SYNTHESIS AND REACTIONS OF PHENYLGLYOXAL ANILS
Prato, Maurizio,Quintily, Ugo,Scorrano, Gianfranco
, p. 405 - 412 (2007/10/02)
Contrary to previous reports, the reaction of anilines and phenylglyoxal in toluene affords the expected anil PhCO-CH=N-Ar, 1.In many cases it is more convenient to carry out the reaction in methanol where the methanol adduct of 1 forms, which may be better isolated, characterised and stored.Since the alcohol adduct is in equilibrium with free 1, it can be used for synthetic purposes as precursor of 1 as in hydrolysis, Diels-Alder, and other reactions initiated by nucleophilic attack on the carbon-nitrogen double bond.
