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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)-

Cyclobutane, 1-chloro-1,2,2-trifluoro-

FC1(Cl)CCC1(F)F Request for Quotation
Chemical Name: Cyclobutane, 1-chloro-1,2,2-trifluoro-
CAS Number: 661-71-2
Product Number: AG003E71(AGN-PC-0JLRS7)
Synonyms:
MDL No:
Molecular Formula: C4H4ClF3
Molecular Weight: 144.5227696

Identification/Properties

Computed Properties
Molecular Weight:
144.521g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
143.995g/mol
Monoisotopic Mass:
143.995g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
114
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


1-Chloro-1,2,2-trifluorocyclobutane, also known as $name$, is a versatile compound widely used in chemical synthesis. Its unique structure and properties make it a valuable reagent in organic chemistry reactions. $name$ is commonly employed as an alkylating agent in various synthetic transformations, where it serves as a source of electrophilic chlorine and fluorine atoms. This reactivity allows $name$ to participate in reactions such as nucleophilic substitution, Grignard reactions, and Friedel-Crafts reactions. Furthermore, $name$ can also act as a building block for the synthesis of complex organic molecules, particularly in the pharmaceutical and agrochemical industries. Its trifluoromethyl and chloro substituents impart specific properties to the resulting compounds, making $name$ a valuable tool for medicinal chemists and synthetic organic chemists alike. Overall, the application of 1-Chloro-1,2,2-trifluorocyclobutane in chemical synthesis highlights its crucial role in modern organic chemistry and its significance in the development of novel compounds with unique properties and functions.