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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-(heptyloxy)-

CCCCCCCOc1ccc(cc1)O Request for Quotation
Chemical Name: Phenol, 4-(heptyloxy)-
CAS Number: 13037-86-0
Product Number: AG000UCL(AGN-PC-0JKIAS)
Synonyms:
MDL No:
Molecular Formula: C13H20O2
Molecular Weight: 208.2967

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
208.301g/mol
XLogP3:
4.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
7
Exact Mass:
208.146g/mol
Monoisotopic Mass:
208.146g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
140
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 4-(Heptyloxy)phenol, also known as heptyloxyphenol, is a versatile chemical that finds wide application in chemical synthesis. It serves as a key building block for creating various compounds with unique properties.Its use in chemical synthesis is particularly valued in the production of advanced materials such as polymers, resins, and pharmaceuticals. By incorporating 4-(Heptyloxy)phenol into the synthesis process, chemists can tailor the properties of the final products to meet specific requirements. The presence of the heptyloxy group imparts desirable characteristics such as increased solubility, stability, and reactivity to the synthesized compounds.Additionally, 4-(Heptyloxy)phenol is utilized in the preparation of specialty chemicals and functional materials due to its ability to introduce specific functionalities and structural motifs into the molecular design. Its role in chemical synthesis extends to the development of innovative technologies in fields such as coatings, adhesives, and personal care products.Overall, the versatile nature of 4-(Heptyloxy)phenol makes it a valuable component in the toolkit of synthetic chemists seeking to create novel compounds with tailored properties and applications.