1. Home
  2. 2,5-Cyclohexadiene-1,4-dione, 2,3,5-trimethyl-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2,5-Cyclohexadiene-1,4-dione, 2,3,5-trimethyl-

O=C1C=C(C)C(=O)C(=C1C)C Request for Quotation
Chemical Name: 2,5-Cyclohexadiene-1,4-dione, 2,3,5-trimethyl-
CAS Number: 935-92-2
Product Number: AG0036QB(AGN-PC-0JL9LF)
Synonyms:
MDL No:
Molecular Formula: C9H10O2
Molecular Weight: 150.1745

Identification/Properties

Properties
MP:
36 °C
BP:
211.72°C (rough estimate)
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Refractive Index:
1.5470 (estimate)
Computed Properties
Molecular Weight:
150.177g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
150.068g/mol
Monoisotopic Mass:
150.068g/mol
Topological Polar Surface Area:
34.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
293
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2,3,5-trimethylbenzo-1,4-quinone is a versatile compound used in various chemical synthesis applications. In organic chemistry, it serves as an important intermediate for the synthesis of various pharmaceuticals, agrochemicals, and specialty compounds. Its unique structure and reactivity make it a valuable building block for the creation of complex organic molecules. Additionally, 2,3,5-trimethylbenzo-1,4-quinone is employed in the production of dyes, polymers, and other specialty chemicals due to its ability to undergo different types of chemical reactions, such as oxidation and reduction, leading to diverse product outcomes. This compound plays a vital role in the development of new materials and innovative chemical processes.