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4-[(3-oxo-3H-isobenzofuran-1-ylidene)methyl]benzoic acid is a complex organic compound characterized by a unique molecular structure. It features a benzoic acid group attached to a 3-oxo-3H-isobenzofuran-1-ylidene system, which is a heterocyclic aromatic ring with a carbonyl group. 4-[(3-oxo-3H-isobenzofuran-1-ylidene)methyl]benzoic acid is known for its potential applications in various chemical and pharmaceutical industries, particularly in the synthesis of certain pharmaceuticals and as a building block for more complex organic molecules. Its chemical properties, such as reactivity and stability, are influenced by the presence of the carbonyl groups and the aromatic rings, making it a subject of interest for researchers in organic chemistry.

964-39-6

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964-39-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 964-39-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 964-39:
(5*9)+(4*6)+(3*4)+(2*3)+(1*9)=96
96 % 10 = 6
So 964-39-6 is a valid CAS Registry Number.

964-39-6Downstream Products

964-39-6Relevant academic research and scientific papers

Phthalazone or phthalazinylphenol derivatives and application thereof

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Paragraph 0048; 0050-0051; 0053, (2018/07/15)

The invention relates to the technical field of chemical synthesis, in particular to phthalazone or phthalazinylphenol derivatives serving as PARP and HDACs double-target inhibitors and application thereof, and aims at providing phthalazone derivatives or phthalazinylphenol derivatives serving as a kind of novel PARP and HDACs double-target inhibitors. The structures of phthalazone or phthalazinylphenol derivatives are shown in formula I or formula II. Phthalazone or phthalazinylphenol derivatives have significant activity of inhibiting poly(ADP-ribose)polymerase and histone deacetylase and have effective anti-tumor effects; new choices are provided for developing and applying anti-tumor drugs related to inhibiting activity of poly(ADP-ribose)polymerase and histone deacetylase. (The formulae are shown in the description.).

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