36713-33-4 Usage
Description
2-(dimethylamino)-1,2-diphenylethanone, also known as benzophenone imine, is an aromatic ketone derivative with the molecular formula C15H15NO. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. Benzophenone imine is a member of the diphenylethanone family of compounds and is used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, dyes, and pigments. It has a strong odor and is considered a skin and eye irritant, requiring careful handling in a well-ventilated area. Additionally, it may pose a health risk through inhalation or ingestion and should be used in accordance with proper safety guidelines.
Uses
Used in Pharmaceutical Industry:
2-(dimethylamino)-1,2-diphenylethanone is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of various medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical industry, 2-(dimethylamino)-1,2-diphenylethanone serves as an intermediate in the production of agrochemicals, aiding in the creation of substances that can protect crops and enhance agricultural productivity.
Used in Dye and Pigment Production:
2-(dimethylamino)-1,2-diphenylethanone is utilized in the production of dyes and pigments due to its chemical properties that allow for the creation of a wide range of colors and shades for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 36713-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,1 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 36713-33:
(7*3)+(6*6)+(5*7)+(4*1)+(3*3)+(2*3)+(1*3)=114
114 % 10 = 4
So 36713-33-4 is a valid CAS Registry Number.
36713-33-4Relevant articles and documents
Superelectrophilic chemistry of amino-nitriles and related substrates
Raja, Erum K.,Klumpp, Douglas A.
experimental part, p. 4494 - 4497 (2011/07/08)
The superacid-promoted Houben/Hoesch reactions of amino-nitriles and related compounds have been studied. The nitriles form dicationic electrophiles and react with benzene in fair to good yields (12-95%). The intermediate iminium ions may also be reduced to the benzylic amines by NaBH4 or H 2.
The reductive coupling of tertiary amides to give enediamines using PhMe2SiLi
Fleming, Ian,Ghosh, Usha,Mack, Stephen R.,Clark, Barry P.
, p. 711 - 712 (2007/10/03)
PhMe2SiLi reacts with tertiary amides to give enediamines, which can be isolated in good yield when the α-carbon is branched; the enediamines can be hydrolysed more or less easily to α-amino ketones, isomerised from Z to E, oxidised to dienedia
