1,2,4-Triphenyl-1,4-butanedione

Base Information

Chemical Name:1,2,4-Triphenyl-1,4-butanedione
CAS No.:4441-01-4
Deprecated CAS:122913-70-6
Molecular Formula:C22H18O2
Molecular Weight:314.384
Hs Code.:2914399090
NSC Number:7759
DSSTox Substance ID:DTXSID30884072
Nikkaji Number:J275.880F
ChEMBL ID:CHEMBL1708985
Mol file:4441-01-4.mol

Synonyms:1,2,4-Triphenyl-1,4-butanedione;4441-01-4;1,2,4-triphenylbutane-1,4-dione;1,4-Butanedione, 1,2,4-triphenyl-;MLS002638027;NSC7759;Desyl-p-acetophenon;1, 1,2,4-triphenyl-;SCHEMBL6201780;CHEMBL1708985;DTXSID30884072;UDJIUKWJBHQMBG-UHFFFAOYSA-N;HMS3093K16;NSC 7759;NSC-7759;ICCB6_000113;MFCD00043773;AKOS015840582;SMR001547529;1,2,4-TRIPHENYLBUTAN-1,4-DIONE;AI3-17642;FT-0606256;FT-0606257

Suppliers and Price of 1,2,4-Triphenyl-1,4-butanedione

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

American Custom Chemicals Corporation
1,2,4-TRIPHENYL-1,4-BUTANEDIONE 95.00%
5G
$ 854.99

Total 6 raw suppliers

Chemical Property of 1,2,4-Triphenyl-1,4-butanedione

Chemical Property:

Vapor Pressure:5.52E-10mmHg at 25°C
Melting Point:126-127oC
Boiling Point:496.2°C at 760 mmHg
Flash Point:183.6°C
PSA：34.14000
Density:1.143g/cm³
LogP:4.92610
XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:6
Exact Mass:314.130679813
Heavy Atom Count:24
Complexity:410

Purity/Quality:

99% ^*data from raw suppliers

1,2,4-TRIPHENYL-1,4-BUTANEDIONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 22-24/25

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(CC(=O)C2=CC=CC=C2)C(=O)C3=CC=CC=C3
General Description 1,2,4-Triphenyl-1,4-butanedione is a diketone compound featuring phenyl substituents at the 1, 2, and 4 positions of a butanedione backbone. It is a synthetic intermediate or target molecule in organic chemistry, often studied for its reactivity in condensation or cyclization reactions due to the presence of two carbonyl groups. 1,2,4-TRIPHENYL-1,4-BUTANEDIONE's structure suggests potential utility in the synthesis of heterocycles or as a precursor for more complex organic frameworks. No further specific chemical or application details are provided in the given context.

Technology Process of 1,2,4-Triphenyl-1,4-butanedione

There total 78 articles about 1,2,4-Triphenyl-1,4-butanedione 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: 100.0%

: 13249-75-7
(Z)-1,2,4-triphenyl-2-butene-1,4-dione

: 4441-01-4
1,2,4-triphenylbutane-1,4-dione

Guidance literature:: With trichlorosilane; Triphenylphosphine oxide; In 1,2-dichloro-ethane; at 25 ℃; for 1h; Reagent/catalyst; Time; Catalytic behavior;
DOI:10.1021/acs.orglett.5b00442

Reference yield: 99.0%

: 100-52-7
benzaldehyde

: 614-47-1
1,3-diphenyl-propen-3-one

: 4441-01-4
1,2,4-triphenylbutane-1,4-dione

Guidance literature:: With 3-mesityl-4,5-dimethyloxazol-3-ium tetraphenylborate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In toluene; at 20 ℃; Schlenk technique; Inert atmosphere;
DOI:10.1021/acs.orglett.8b02636

Reference yield: 97.0%

: 1310823-53-0
(Z)-1,3,4,5-tetraphenylpent-4-en-1-one

: 4441-01-4
1,2,4-triphenylbutane-1,4-dione

Guidance literature:: (Z)-1,3,4,5-tetraphenylpent-4-en-1-one; With ozone; In dichloromethane; at -78 ℃; Inert atmosphere;

With triphenylphosphine; In dichloromethane; at -78 - 20 ℃; Inert atmosphere;
DOI:10.1021/ol201133n