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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)-

2,3-Butanediol, 1,1,1,4,4,4-hexafluoro-2,3-bis(trifluoromethyl)-

OC(C(C(F)(F)F)(C(F)(F)F)O)(C(F)(F)F)C(F)(F)F Request for Quotation
Chemical Name: 2,3-Butanediol, 1,1,1,4,4,4-hexafluoro-2,3-bis(trifluoromethyl)-
CAS Number: 918-21-8
Product Number: AG003QW2(AGN-PC-0JKB7N)
Synonyms:
MDL No:
Molecular Formula: C6H2F12O2
Molecular Weight: 334.0597184

Identification/Properties

Properties
MP:
18 °C
BP:
129 °C
Storage:
Room Temperature;Keep in dry area;
Form:
Liquid
Refractive Index:
1.3102
Computed Properties
Molecular Weight:
334.061g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
14
Rotatable Bond Count:
1
Exact Mass:
333.986g/mol
Monoisotopic Mass:
333.986g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
292
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


The chemical 2,3-Butanediol, 1,1,1,4,4,4-hexafluoro-2,3-bis(trifluoromethyl) plays a crucial role in chemical synthesis, particularly in the field of organic chemistry. Its unique chemical properties make it a valuable reagent for a variety of reactions. This compound is often utilized as a versatile building block for the synthesis of complex organic molecules due to its ability to participate in multiple types of chemical transformations.One of the key applications of 2,3-Butanediol, 1,1,1,4,4,4-hexafluoro-2,3-bis(trifluoromethyl) is as a fluorinated synthon in the preparation of fluorine-containing organic compounds. Its trifluoromethyl groups provide a valuable source of fluorine atoms, which can be strategically incorporated into target molecules to modulate their physical and chemical properties. This compound is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and materials science, where the introduction of fluorine can enhance biological activity, stability, and other important characteristics.Furthermore, 2,3-Butanediol, 1,1,1,4,4,4-hexafluoro-2,3-bis(trifluoromethyl) can serve as a protecting group in organic synthesis to selectively block reactive functional groups and direct chemical reactions towards specific sites on a molecule. By strategically deploying this compound as a protecting group, chemists can control the reactivity and selectivity of synthetic transformations, enabling the efficient construction of complex molecular frameworks.In summary, the versatile nature of 2,3-Butanediol, 1,1,1,4,4,4-hexafluoro-2,3-bis(trifluoromethyl) makes it a valuable tool in chemical synthesis, allowing chemists to access a wide range of fluorinated compounds and manipulate molecular structures with precision and control.