36713-33-4 Usage
General Description
2-(dimethylamino)-1,2-diphenylethanone, also known as benzophenone imine, is a chemical compound with the molecular formula C15H15NO. It is an aromatic ketone derivative and a member of the diphenylethanone family of compounds. Benzophenone imine is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. It is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and also finds applications in the production of dyes and pigments. 2-(dimethylamino)-1,2-diphenylethanone is known to have a strong odor and is considered to be a skin and eye irritant, and should be handled with care 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.
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
