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3-Phenylsuccinaldehydic acid, also known as 3-phenyl-4-oxo-4-phenylbutanoic acid, is a chemical compound with the molecular formula C14H12O3. It is a derivative of succinic acid, featuring a phenyl group attached to the third carbon atom and an aldehyde group at the fourth carbon. This organic compound is characterized by its aromatic structure and is used in the synthesis of various pharmaceuticals and chemical intermediates. It is a white crystalline solid that is soluble in organic solvents and has a melting point of approximately 150-152°C. Due to its reactivity, 3-phenylsuccinaldehydic acid is often employed in the preparation of complex organic molecules and can be further functionalized through various chemical reactions.

5676-35-7

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5676-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5676-35-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,7 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5676-35:
(6*5)+(5*6)+(4*7)+(3*6)+(2*3)+(1*5)=117
117 % 10 = 7
So 5676-35-7 is a valid CAS Registry Number.

5676-35-7Downstream Products

5676-35-7Relevant academic research and scientific papers

Lactone Chemistry. Synthesis of β-Substituted, γ-Functionalized Butanolides and Butenolides and Succinaldehydic Acids from Glyoxylic Acid

Bourguignon, J. J.,Wermuth, C. G.

, p. 4889 - 4894 (2007/10/02)

The Mannich-type aminoalkylation reaction of enolizable aldehydes with morpholine and glyoxylic acid instead of formaldehyde was investigated: in basic and neutral media were obtained α,γ-dimorpholinobutanolides 2 and α-morpholino-γ-hydroxybutanolides 1, respectively.In acidic medium the spontaneous elimination of the α-morpholino group afforded the γ-hydroxybutenolide 8.The reaction pathways were suggested from the isolation and characterization of some intermediates of the Mannich reaction.These lactone structures constitute versatile synthetic intermediates for the preparation of β-substituted succinaldehydic acids 15 and 5-substituted 3-(2H)-pyridazinones 13 and 14.

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