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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-methoxy-4-(2-propenyl)-

COc1ccc(cc1)CC=C Request for Quotation
Chemical Name: Benzene, 1-methoxy-4-(2-propenyl)-
CAS Number: 140-67-0
Product Number: AG003KN5(AGN-PC-0JK8QL)
Synonyms:
MDL No:
Molecular Formula: C10H12O
Molecular Weight: 148.2017

Identification/Properties

Properties
MP:
25°C
BP:
215.5°C
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Refractive Index:
n20/D 1.521(lit.)
Solubility:
0.178g/l
Computed Properties
Molecular Weight:
148.205g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
148.089g/mol
Monoisotopic Mass:
148.089g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
112
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-H350-H360
Precautionary Statements:
P301+P312+P330
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Allylanisole, also known as p-allylanisole, is a versatile compound frequently utilized in chemical synthesis as a key building block for various organic reactions. This compound serves as a valuable starting material in the production of numerous specialized chemicals with diverse applications across the pharmaceutical, fragrance, and agrochemical industries.In chemical synthesis, 4-Allylanisole plays a crucial role as a reactant in the formation of more complex molecules through processes such as allylation and cross-coupling reactions. Its allyl group provides a significant degree of reactivity, enabling the introduction of functional groups and modifications to the molecular structure. This compound's unique properties make it an attractive option for chemists seeking to create new compounds with specific properties and applications.Furthermore, 4-Allylanisole is commonly employed in the synthesis of fragrances and flavoring agents due to its distinctive aromatic profile. Its presence in these formulations can enhance the overall olfactory characteristics of the final product, making it a popular choice for perfumers and flavor chemists seeking to develop unique and appealing scents.In addition to its role in fragrance and flavor chemistry, 4-Allylanisole also finds application in the synthesis of biologically active compounds, making it a valuable tool in pharmaceutical research and drug development. By incorporating this compound into various synthetic pathways, chemists can access diverse chemical starting points for the creation of potential drug candidates with specific therapeutic properties.Overall, the versatile nature of 4-Allylanisole makes it an essential component in the toolkit of synthetic chemists, offering a wide range of possibilities for the creation of novel chemical compounds with applications spanning multiple industries.