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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)-

2,3-Dimethyl-2,3-Diphenylbutane

CC(C(c1ccccc1)(C)C)(c1ccccc1)C Request for Quotation
Chemical Name: 2,3-Dimethyl-2,3-Diphenylbutane
CAS Number: 1889-67-4
Product Number: AG002HHL(AGN-PC-0WA5MQ)
Synonyms:
MDL No:
Molecular Formula: C18H22
Molecular Weight: 238.3673

Identification/Properties

Computed Properties
Molecular Weight:
238.374g/mol
XLogP3:
5.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
3
Exact Mass:
238.172g/mol
Monoisotopic Mass:
238.172g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
221
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3-Dimethyl-2,3-diphenylbutane, a versatile compound used in chemical synthesis, serves as a valuable building block in organic chemistry reactions. Known for its unique structural properties, this molecule is strategically employed to participate in the formation of various complex organic compounds through multi-step synthetic routes. By acting as a key intermediate, 2,3-Dimethyl-2,3-diphenylbutane contributes to the creation of diverse functional molecules with tailored physical and chemical characteristics that are essential in the development of advanced materials, pharmaceuticals, and agrochemicals. In the realm of organic synthesis, the strategic incorporation of 2,3-Dimethyl-2,3-diphenylbutane enables chemists to design and execute sophisticated pathways for the construction of novel molecular structures with enhanced properties, thus facilitating innovation and progress in the field of chemistry.