4,4'-Bis(trimethylacetoxy)benzophenone

Base Information

Chemical Name:4,4'-Bis(trimethylacetoxy)benzophenone
CAS No.:112004-83-8
Molecular Formula:C23H26O5
Molecular Weight:382.456
Hs Code.:
European Community (EC) Number:632-715-4
ChEMBL ID:CHEMBL10541
DSSTox Substance ID:DTXSID30408474
Pharos Ligand ID:QVV83PXC9SHX
Wikidata:Q82213962
Mol file:112004-83-8.mol

Synonyms:112004-83-8;4,4'-BIS(TRIMETHYLACETOXY)BENZOPHENONE;Carbonylbis(4,1-phenylene) bis(2,2-dimethylpropanoate);4,4'-dipivaloyloxybenzophenone;[4-[4-(2,2-dimethylpropanoyloxy)benzoyl]phenyl] 2,2-dimethylpropanoate;CHEMBL10541;SCHEMBL4639551;DTXSID30408474;BDBM50023545;MFCD03932084;AKOS024406556;2,2-Dimethyl-propanoic Acid 4-[4-(2,2-Dimethyl-1-oxopropoxy)benzoyl]phenyl Ester;AS-82153;D5620;FT-0663403;T71602;Carbonylbis(4,1-phenylene)bis(2,2-dimethylpropanoate);(Oxomethanediyl)dibenzene-4,1-diyl bis(2,2-dimethylpropanoate);4,4 inverted exclamation mark -Bis(trimethylacetoxy)benzophenone;4-(4-((2,2-DIMETHYLPROPANOYL)OXY)BENZOYL)PHENYL PIVALATE;4-[4-(1,1-Dimethylethylcarbonyloxy)benzoyl]phenyl 2,2-dimethylpropanoate;2,2-Dimethyl-propionic acid 4-[4-(2,2-dimethyl-propionyloxy)-benzoyl]-phenyl ester

Suppliers and Price of 4,4'-Bis(trimethylacetoxy)benzophenone

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
4,4’-Bis(trimethylacetoxy)benzophenone
25mg
$ 80.00

TCI Chemical
4,4'-Dipivaloyloxybenzophenone
1G
$ 28.00

TCI Chemical
4,4'-Dipivaloyloxybenzophenone
5G
$ 84.00

Biosynth Carbosynth
4,4'-Bis(trimethylacetoxy)benzophenone
25 mg
$ 125.00

Biosynth Carbosynth
4,4'-Bis(trimethylacetoxy)benzophenone
50 mg
$ 227.00

Biosynth Carbosynth
4,4'-Bis(trimethylacetoxy)benzophenone
100 mg
$ 413.00

Biosynth Carbosynth
4,4'-Bis(trimethylacetoxy)benzophenone
500 mg
$ 1365.00

Biosynth Carbosynth
4,4'-Bis(trimethylacetoxy)benzophenone
250 mg
$ 752.50

American Custom Chemicals Corporation
4,4'-BIS(TRIMETHYLACETOXY)BENZOPHENONE 95.00%
500MG
$ 1732.50

American Custom Chemicals Corporation
4,4'-BIS(TRIMETHYLACETOXY)BENZOPHENONE 95.00%
50MG
$ 721.88

Total 9 raw suppliers

Chemical Property of 4,4'-Bis(trimethylacetoxy)benzophenone

Chemical Property:

Vapor Pressure:6.05E-10mmHg at 25°C
Melting Point:173-174°C
Boiling Point:495.2°C at 760 mmHg
Flash Point:213.3°C
PSA：69.67000
Density:1.118g/cm³
LogP:4.82060
Solubility.:Dichloromethane, Ethyl Acetate, Methanol
XLogP3:5.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:382.17802393
Heavy Atom Count:28
Complexity:515

Purity/Quality:

97% ^*data from raw suppliers

4,4’-Bis(trimethylacetoxy)benzophenone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)C(=O)OC1=CC=C(C=C1)C(=O)C2=CC=C(C=C2)OC(=O)C(C)(C)C

Technology Process of 4,4'-Bis(trimethylacetoxy)benzophenone

There total 2 articles about 4,4'-Bis(trimethylacetoxy)benzophenone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 91.0%

: 611-99-4
4,4'-Dihydroxybenzophenone

: 3282-30-2
pivaloyl chloride

: 112004-83-8
[4-[4-(2,2-dimethylpropanoyloxy)benzoyl]phenyl] 2,2-dimethylpropanoate

Guidance literature:: With triethylamine; In tetrahydrofuran; dichloromethane; at 20 ℃;
DOI:10.1016/j.ejmech.2016.04.076

Reference yield:

: 611-99-4
4,4'-Dihydroxybenzophenone

: 3282-30-2
pivaloyl chloride

: 114031-67-3
[4-(4-hydroxybenzoyl)phenyl]-2,2-dimethyl propanoate

: 112004-83-8
[4-[4-(2,2-dimethylpropanoyloxy)benzoyl]phenyl] 2,2-dimethylpropanoate

Guidance literature:: With sodium hydride; Yield given. Multistep reaction. Yields of byproduct given; 1.) THF, mineral oil, room temperature, 30 min, 2.) THF, mineral oil, 2 h;
DOI:10.1021/jo952279l