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5-Morpholin-4-yl-4-phenyl-5H-furan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78939-67-0

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78939-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78939-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,3 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78939-67:
(7*7)+(6*8)+(5*9)+(4*3)+(3*9)+(2*6)+(1*7)=200
200 % 10 = 0
So 78939-67-0 is a valid CAS Registry Number.

78939-67-0Relevant academic research and scientific papers

Histone deacetylase inhibitor taking pyridazinone as mother nucleus structure, and preparation method and applications thereof

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Paragraph 0398-0401, (2019/02/10)

The invention discloses a histone deacetylase inhibitor taking pyridazinone as a mother nucleus structure, and a preparation method and applications thereof. The structure of the inhibitor is shown asa formula I; and the compound shown as the formula I has good histone deacetylase inhibitory activity and anti-tumor cell proliferation effects, and can be used for treating cancers. The structure ofthe inhibitor is shown as the formula I.

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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