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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-methoxyphenyl)ethynyl]-4-propyl-

CCCc1ccc(cc1)C#Cc1ccc(cc1)OC Request for Quotation
Chemical Name: Benzene, 1-[(4-methoxyphenyl)ethynyl]-4-propyl-
CAS Number: 39969-26-1
Product Number: AG003B0W(AGN-PC-03VUSI)
Synonyms:
MDL No:
Molecular Formula: C18H18O
Molecular Weight: 250.3349

Identification/Properties

Properties
BP:
162-164°C at 1 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
250.341g/mol
XLogP3:
5.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
5
Exact Mass:
250.136g/mol
Monoisotopic Mass:
250.136g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
305
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#:
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


1-Methoxy-4-((4-propylphenyl)ethynyl)benzene is a versatile compound widely utilized in chemical synthesis applications. As a key building block in organic chemistry, this compound is commonly employed in the construction of complex molecular structures due to its unique reactivity and functional groups. Its ethynyl and propylphenyl moieties can serve as anchor points for further modifications, allowing for the creation of novel compounds with tailored properties. In the realm of drug discovery, 1-Methoxy-4-((4-propylphenyl)ethynyl)benzene plays a crucial role in the development of pharmaceuticals and biologically active molecules. Its precise chemical structure allows for precise manipulation and fine-tuning of desired pharmacological properties, making it an indispensable tool for medicinal chemists. Furthermore, in materials science, this compound is valued for its ability to participate in various cross-coupling reactions and polymerization processes, enabling the synthesis of advanced materials with specific functionalities. Overall, the diverse applications of 1-Methoxy-4-((4-propylphenyl)ethynyl)benzene highlight its significance in advancing the field of chemical synthesis.