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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-chlorotetrahydro-

ClC1CCOCC1 Request for Quotation
Chemical Name: 2H-Pyran, 4-chlorotetrahydro-
CAS Number: 1768-64-5
Product Number: AG0024X5(AGN-PC-0JMPBU)
Synonyms:
MDL No:
Molecular Formula: C5H9ClO
Molecular Weight: 120.5774

Identification/Properties

Properties
BP:
150°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.462(lit.)
Solubility:
water: soluble(lit.)
Computed Properties
Molecular Weight:
120.576g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
120.034g/mol
Monoisotopic Mass:
120.034g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
50
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chlorotetrahydro-2H-pyran, also known as 4-chlorooxane, is a versatile compound widely utilized in chemical synthesis for various applications. This compound serves as a key building block in the production of pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, 4-Chlorotetrahydro-2H-pyran acts as a valuable intermediate in the creation of complex organic molecules. Its unique chemical structure and reactivity make it an essential component in the synthesis of heterocyclic compounds, which are commonly found in drugs and bioactive molecules. By incorporating 4-Chlorotetrahydro-2H-pyran into synthetic pathways, chemists can introduce specific functional groups and stereochemistry into their target molecules with precision and efficiency.Additionally, 4-Chlorotetrahydro-2H-pyran can be functionalized further to tailor its properties for specific applications. Its chlorine atom can serve as a handle for further derivatization, allowing for the introduction of additional substituents or functional groups to modulate the compound's activity or properties. This versatility makes 4-Chlorotetrahydro-2H-pyran an indispensable tool in the arsenal of synthetic chemists working in drug discovery, material science, and other research fields.