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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, 1,1'-(1-methyl-1,3-propanediyl)bis-

CC(c1ccccc1)CCc1ccccc1 Request for Quotation
Chemical Name: Benzene, 1,1'-(1-methyl-1,3-propanediyl)bis-
CAS Number: 1520-44-1
Product Number: AG003D4S(AGN-PC-0JKC5I)
Synonyms:
MDL No:
Molecular Formula: C16H18
Molecular Weight: 210.3141

Identification/Properties

Properties
BP:
295.1°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
210.32g/mol
XLogP3:
5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
4
Exact Mass:
210.141g/mol
Monoisotopic Mass:
210.141g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
173
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The Butane-1,3-diyldibenzene compound is a versatile building block in organic synthesis, commonly utilized in the creation of complex chemical structures. This compound serves as a crucial intermediate in various organic reactions, particularly in the production of pharmaceuticals, agrochemicals, and advanced materials. Its unique chemical properties enable it to participate in key reactions such as cross-coupling reactions, hydrogenation, and functional group transformations. Through strategic manipulation of its molecular structure, chemists can harness the reactivity of Butane-1,3-diyldibenzene to facilitate the synthesis of diverse compounds with targeted properties and functionalities. Its role in chemical synthesis extends to the development of new materials, catalysts, and bioactive molecules, highlighting its significance in advancing scientific research and innovation.