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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)-

Benzene, (3-methylbutyl)-

CC(CCc1ccccc1)C Request for Quotation
Chemical Name: Benzene, (3-methylbutyl)-
CAS Number: 2049-94-7
Product Number: AG0029QX(AGN-PC-004KY4)
Synonyms:
MDL No:
Molecular Formula: C11H16
Molecular Weight: 148.2447

Identification/Properties

Properties
MP:
-44.72℃ (estimate)
BP:
195.0°C
Storage:
Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
148.249g/mol
XLogP3:
4.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
3
Exact Mass:
148.125g/mol
Monoisotopic Mass:
148.125g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
88.2
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:
H227-H302
Precautionary Statements:
P210-P280-P370+P378-P403+P235-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Isopentylbenzene, also known as isopropylbenzene or cumene, is a vital intermediate chemical compound widely utilized in various chemical synthesis processes. This versatile compound plays a crucial role in the production of phenol and acetone through the cumene process. By undergoing oxidation and decomposition reactions, isopentylbenzene can be efficiently converted into phenol and acetone, which are essential building blocks in the manufacturing of numerous industrial chemicals and plastics.Additionally, isopentylbenzene serves as a key starting material in the synthesis of various pharmaceutical compounds, fragrances, and agrochemicals. Its unique chemical structure and reactivity make it a valuable precursor in organic synthesis, allowing for the creation of diverse molecules with specific functions and properties.Moreover, Isopentylbenzene's ability to undergo alkylation and acylation reactions makes it an essential reagent in the preparation of specialty chemicals and high-performance materials. Its involvement in the synthesis of polymers, resins, and additives further demonstrates its significance in the chemical industry.Overall, Isopentylbenzene's versatile applications in chemical synthesis highlight its importance as a foundational compound that enables the production of a wide range of valuable products across various industrial sectors.