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Chemical structure of CAS 120-46-7

Dibenzoylmethane

In Stock•Starting at $6 for 25 g•Purity ≥ 98%
CAS No.120-46-7
MDL No.MFCD00003085
MFC15H12O2
MW224.25
InChI KeyNZZIMKJIVMHWJC-UHFFFAOYSA-N
CUSTOM SYNTHESIS

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
25 g98%$6In Stock
100 g98%$9In Stock
200 g98%$16In Stock
500 g98%$18In Stock
1 kg98%$33In Stock
5 kg98%$143In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

Dibenzoylmethane is a beta-diketone derived from acetylacetone by replacing both methyl groups with phenyl groups. It is a minor component of licorice root extract (Glycyrrhiza glabra) and exhibits antimutagenic and anticancer properties. It functions as an antineoplastic agent, metabolite, and antimutagen. It is also classified as an aromatic ketone.

CAS No.120-46-7
Product NameDibenzoylmethane
IrritantIrritant
Signal Word:Warning
HCode:H317
PCode:P261-P272-P280-P302+P352-P321-P333+P317-P362+P364-P501

Related Articles

Studies related to this compound and its mechanism of action

Bridging nitrate groups in [Mn(4)O(3)(NO(3))(O(2)CMe)(3)(R(2)dbm)(3)] (R = H, Et) and [Mn(4)O(2)(NO(3))(O(2)CEt)(6)(bpy)(2)](ClO(4)): acidolysis routes to tetranuclear manganese carboxylate complexes.

Inorganic chemistry • Vol. 41, Issue 4 • 2002
PMID: 11849081DOI: 10.1021/ic0105617

Dibenzoylmethane induces cell cycle deregulation in human prostate cancer cells.

Cancer letters • Vol. 178, Issue 2 • 2002
PMID: 11867200DOI: 10.1016/s0304-3835(01)00844-8

Practical synthesis of optically active amino alcohols via asymmetric transfer hydrogenation of functionalized aromatic ketones.

The Journal of organic chemistry • Vol. 67, Issue 5 • 2002
PMID: 11871912DOI: 10.1021/jo011076w

Cytotoxic flavonoids from the stem bark of Lonchocarpus aff. fluvialis.

Phytotherapy research : PTR • Vol. 16, Issue 4 • 2002
PMID: 12112286DOI: 10.1002/ptr.889

Documentation

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