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Diphenylacetaldehyde imine, also known as N-phenylbenzaldimine, is an organic compound with the chemical formula C13H11N. It is formed by the condensation of benzaldehyde with aniline, resulting in a Schiff base. This colorless to pale yellow crystalline solid is soluble in organic solvents such as ethanol and ether. Diphenylacetaldehyde imine is an important intermediate in the synthesis of various pharmaceuticals, dyes, and polymers, due to its ability to undergo a range of chemical reactions, including reduction, oxidation, and condensation. It is also used as a reagent in analytical chemistry for the detection of certain metal ions. The compound is typically synthesized through the reaction of benzaldehyde with aniline in the presence of an acid catalyst, and its structure is characterized by a double bond between the nitrogen and carbon atoms, giving it imine functionality.

947-89-7

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947-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 947-89-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 947-89:
(5*9)+(4*4)+(3*7)+(2*8)+(1*9)=107
107 % 10 = 7
So 947-89-7 is a valid CAS Registry Number.

947-89-7Relevant academic research and scientific papers

Metal-free, one-pot oxidative conversion of aldehydes to primary thioamides in aqueous media

Yadav, Arvind K.,Srivastava, Vishnu P.,Yadav, Lal Dhar S.

, p. 408 - 416 (2014)

One-pot tandem reactions of a variety of aldehydes with aqueous ammonia, molecular iodine, and O,O-diethyl dithiophosphoric acid readily afford the corresponding primary thioamides. This is an inexpensive, practical, and metal-free way of accessing various thioamides from aldehydes in aqueous media. The pure products are obtained simply by filtration followed by successive washing with aqueous sodium thiosulfate and water. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications for the following free supplemental resource(s): Full experimental and spectral details.]

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