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159611

Sigma-Aldrich

4,4′-Dimethoxybenzil

98%

Synonym(s):

p-Anisil, Di-p-anisoyl

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About This Item

Linear Formula:
CH3OC6H4COCOC6H4OCH3
CAS Number:
1226-42-2
Molecular Weight:
270.28
Beilstein:
531345
EC Number:
214-960-5
MDL number:
MFCD00008405
UNSPSC Code:
12352100
PubChem Substance ID:
24849827
NACRES:
NA.22

Assay

98%

form

solid

mp

132-134 °C (lit.)

SMILES string

COc1ccc(cc1)C(=O)C(=O)c2ccc(OC)cc2

InChI

1S/C16H14O4/c1-19-13-7-3-11(4-8-13)15(17)16(18)12-5-9-14(20-2)10-6-12/h3-10H,1-2H3

InChI key

YNANGXWUZWWFKX-UHFFFAOYSA-N

Gene Information

human ... ACHE(43) , BCHE(590) , CES1(1066)

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General description

Mesomorphic properties of a substituted bis(dithiolene)nickel complex derived from 4,4′-dimethoxybenzil has been reported. Diffuse scattering in 4,4′-dimethoxybenzil has been studied via Monte Carlo computer-simulation model.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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T R Welberry et al.
Acta crystallographica. Section B, Structural science, 59(Pt 6), 760-769 (2003-11-25)
A recently developed method for fitting a Monte Carlo computer-simulation model to observed single-crystal diffuse X-ray scattering has been used to study the diffuse scattering in 4,4'-dimethoxybenzil, C16H14O4. A model involving only nine parameters, consisting of seven intermolecular force constants
Chiann-Tyng Chou et al.
Journal of chromatography. A, 1043(2), 255-263 (2004-08-28)
The preparation and mesomorphic properties of a substituted bis(dithiolene)nickel complex derived from 4, 4'-dimethoxybenzil are reported. The phase transition temperatures were based on data obtained by polarized light microscopy and differential scanning calorimetry. The mesogenic phase existed over the temperature
J R de la Fuente et al.
Journal of bioluminescence and chemiluminescence, 7(1), 27-35 (1992-01-01)
The pyrolyisis of di-tert-butyl peroxyoxalate in the presence of para-substituted benzaldehydes produces almost quantitatively the corresponding p,p'-disubstituted benzils. The formation of these products is accompanied by chemiluminescence arising from excited triplets. From the quantum yield of excited triplet generation and

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