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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)-

Phenol, 4-cyclopropyl-

Oc1ccc(cc1)C1CC1 Request for Quotation
Chemical Name: Phenol, 4-cyclopropyl-
CAS Number: 10292-61-2
Product Number: AG007J20(AGN-PC-0NDZ6P)
Synonyms:
MDL No:
Molecular Formula: C9H10O
Molecular Weight: 134.1751

Identification/Properties

Computed Properties
Molecular Weight:
134.178g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
134.073g/mol
Monoisotopic Mass:
134.073g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
110
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#:
2430
Hazard Statements:
H303-H314-H371-H373-H411
Precautionary Statements:
P501-P273-P260-P270-P264-P280-P391-P308+P311-P303+P361+P353-P301+P330+P331-P363-P304+P340+P310-P305+P351+P338+P310-P405
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Cyclopropylphenol is a versatile compound widely used in chemical synthesis as an important building block for various organic reactions. Its unique structure, characterized by the presence of a cyclopropyl group attached to a phenolic ring, imparts distinct reactivity and properties that make it valuable in different synthetic pathways.One key application of 4-Cyclopropylphenol is as a precursor for the synthesis of biologically active compounds and pharmaceuticals. Its ability to undergo various functional group transformations, such as halogenation, alkylation, and acylation, allows for the creation of a diverse array of derivatives with potential medicinal properties. These derivatives can be further utilized in the development of new drugs or bioactive molecules for therapeutic purposes.Additionally, 4-Cyclopropylphenol serves as a useful intermediate in the preparation of specialty chemicals, agrochemicals, and materials. Its role in multi-step synthesis routes enables the construction of complex molecular structures with specific functionalities tailored for different applications in industry. By incorporating 4-Cyclopropylphenol into synthetic sequences, chemists can access novel compounds with desired properties for a wide range of uses.Overall, 4-Cyclopropylphenol plays a crucial role in the field of chemical synthesis by offering a platform for the construction of diverse molecules with potential applications in pharmaceuticals, materials science, and various other industries. Its versatility and reactivity make it a valuable tool for creating intricate molecular architectures and advancing knowledge in organic chemistry.