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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, 1,4-bis(1,1-dimethylethyl)-

CC(c1ccc(cc1)C(C)(C)C)(C)C Request for Quotation
Chemical Name: Benzene, 1,4-bis(1,1-dimethylethyl)-
CAS Number: 1012-72-2
Product Number: AG0003XQ(AGN-PC-0JKBFS)
Synonyms:
MDL No:
Molecular Formula: C14H22
Molecular Weight: 190.3245

Identification/Properties

Properties
MP:
76-78 °C
BP:
236°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.4955 (estimate)
Computed Properties
Molecular Weight:
190.33g/mol
XLogP3:
5.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
2
Exact Mass:
190.172g/mol
Monoisotopic Mass:
190.172g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
147
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:
Danger
UN#:
3077
Hazard Statements:
H410
Precautionary Statements:
P273-P391-P501
Class:
9
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,4-Di-tert-butylbenzene, also known as DTBB, is a versatile compound widely utilized in chemical synthesis. This aromatic compound is valued for its unique structure and properties, making it ideal for various applications in the field of organic chemistry.In chemical synthesis, 1,4-Di-tert-butylbenzene serves as a valuable building block for the preparation of a range of complex molecules. Its bulky tert-butyl groups provide steric hindrance, which can influence the reactivity and selectivity of certain reactions. This compound can act as a protecting group in organic synthesis, shielding reactive functional groups from unwanted side reactions.Additionally, 1,4-Di-tert-butylbenzene can be used as a starting material for the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its high level of purity and stability make it a reliable candidate for use in the synthesis of fine chemicals where control over stereochemistry and regioselectivity is crucial.Overall, 1,4-Di-tert-butylbenzene plays a significant role in modern chemical synthesis as a key intermediate with diverse applications in the preparation of complex organic molecules.