90-96-0 | Bis(4-Methoxyphenyl)methanone

Packsize	Purity	Availability	Price	Discounted Price
25g	98%	in stock	$14.00	$10.00
100g	98%	in stock	$30.00	$21.00
500g	98%	in stock	$114.00	$80.00

Description

• Catalog Number: AB44769
• Chemical Name: Bis(4-Methoxyphenyl)methanone
• CAS Number: 90-96-0
• Molecular Formula: C15H14O3
• Molecular Weight: 242.2699
• MDL Number: MFCD00008404
• SMILES: COc1ccc(cc1)C(=O)c1ccc(cc1)OC
• NSC Number: 4191

Computed Properties

• Complexity: 235
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• XLogP3: 3.6

Literature

• Photobehavior of mixed nπ*/ππ* triplets: simultaneous detection of the two transients, solvent-dependent hydrogen abstraction, and reequilibration upon protein binding.

  The journal of physical chemistry. B 20110915

• Asymmetric Rh(II)-catalyzed cyclopropanation of alkenes with diacceptor diazo compounds: p-methoxyphenyl ketone as a general stereoselectivity controlling group.

  Journal of the American Chemical Society 20110615

• Microphotochemistry: 4,4'-Dimethoxybenzophenone mediated photodecarboxylation reactions involving phthalimides.

  Beilstein journal of organic chemistry 20110101

• Experimental and theoretical studies on the mechanism of photochemical hydrogen transfer from 2-aminobenzimidazole to nπ* and ππ* aromatic ketones.

  The journal of physical chemistry. B 20100916

• 4,4'-Dimethoxy-benzophenone: a triclinic polymorph.

  Acta crystallographica. Section E, Structure reports online 20080701

• Oxygen acidity of ring methoxylated 1,1-diarylalkanol radical cations bearing alpha-cyclopropyl groups. The competition between O-neophyl shift and C-cyclopropyl beta-scission in the intermediate 1,1-diarylalkoxyl radicals.

  The Journal of organic chemistry 20060414

• Dual electron transfer pathways from 4,4'-dimethoxybenzophenone ketyl radical in the excited state to parent molecule in the ground state.

  The journal of physical chemistry. A 20050811

• Oxidative dechlorination of methoxychlor by ligninolytic enzymes from white-rot fungi.

  Chemosphere 20040401