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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)-

2H-Pyran-4-ol, tetrahydro-2-phenyl-

OC1CCOC(C1)c1ccccc1 Request for Quotation
Chemical Name: 2H-Pyran-4-ol, tetrahydro-2-phenyl-
CAS Number: 132149-01-0
Product Number: AG0010A7(AGN-PC-002DGQ)
Synonyms:
MDL No:
Molecular Formula: C11H14O2
Molecular Weight: 178.2277

Identification/Properties

Computed Properties
Molecular Weight:
178.231g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
178.099g/mol
Monoisotopic Mass:
178.099g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
152
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Phenyltetrahydro-2H-pyran-4-ol, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block and reagent. Its unique structure lends itself to various synthetic pathways, making it a valuable asset in the creation of complex organic molecules.This compound can be utilized in the formation of innovative pharmaceuticals, agricultural chemicals, and advanced materials. In chemical synthesis, $name$ serves as a key intermediate for the synthesis of biologically active compounds, fragrances, and flavoring agents.Its reactivity allows for selective functional group transformations and efficient construction of intricate molecular structures. By incorporating $name$ into synthetic routes, chemists can achieve precise control over stereochemistry and regioselectivity, leading to enhanced efficiency in the synthesis of target molecules.Moreover, the versatile nature of 2-Phenyltetrahydro-2H-pyran-4-ol enables its use in the development of novel synthetic methodologies and strategies. Its diverse applications make it a valuable tool for chemists seeking to explore new avenues in the field of organic synthesis.