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2',4',5'-Tribenzyloxyacetophenone is an organic compound with the molecular formula C27H24O3. It is a derivative of acetophenone, where three benzyloxy groups are attached to the 2', 4', and 5' positions of the phenyl ring. 2',4',5'-tribenzyloxyacetophenone is characterized by its aromatic structure and the presence of a ketone group, which is a carbonyl group (C=O) bonded to an alkyl group. The benzyloxy groups contribute to the compound's lipophilic nature, making it soluble in organic solvents. It is often used in organic synthesis as a protecting group for phenols, particularly in the synthesis of complex molecules where selective protection of hydroxyl groups is required. The compound is also of interest in the field of materials science for its potential applications in the development of new polymers and other advanced materials.

7298-38-6

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7298-38-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7298-38-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,9 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7298-38:
(6*7)+(5*2)+(4*9)+(3*8)+(2*3)+(1*8)=126
126 % 10 = 6
So 7298-38-6 is a valid CAS Registry Number.

7298-38-6Downstream Products

7298-38-6Relevant academic research and scientific papers

Inhibitors for expression of IgE receptor on human mast cell from Puerariae Flos

Tamura, Satoru,Yoshihira, Kunichika,Tokumaru, Mariko,Zisheng, Xu,Murakami, Nobutoshi

scheme or table, p. 3872 - 3875 (2010/08/19)

Bioassay-guided separation of the extract of the medicinal plant, Puerariae Flos, disclosed the two isoflavones tectorigenin (1) and genistein (2) as the inhibitors for expression of IgE receptor (FcRI), the key molecule triggering the allergic reactions, on human mast cells. As a result of analysis of structure-activity relationship of the naturally occurring and synthesized isoflavones, 7-O-methyl glycitein (11) was disclosed as the more potent inhibitor than tectorigenin (1). These isoflavone ingredients suppressed expression of FcRI more potently than the active flavonoids found previously. In addition, tectorigenin (1) was clarified to particularly reduce generation of γ-chain subunit to suppress expression of FcRI among the three subunits.

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