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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)-

Cyclopropaneacetic acid, 2,2-difluoro-

OC(=O)CC1CC1(F)F Request for Quotation
Chemical Name: Cyclopropaneacetic acid, 2,2-difluoro-
CAS Number: 123131-67-9
Product Number: AG000K2I(AGN-PC-001HFW)
Synonyms:
MDL No:
Molecular Formula: C5H6F2O2
Molecular Weight: 136.0967

Identification/Properties

Computed Properties
Molecular Weight:
136.098g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
136.034g/mol
Monoisotopic Mass:
136.034g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
144
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

GHS Pictogram:
Signal Word:
Danger
UN#:
3261
Hazard Statements:
H302-H314
Precautionary Statements:
P261-P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,​2-​Difluorocyclopropane​acetic acid is a versatile compound that finds wide application in chemical synthesis due to its unique structural properties. This compound is utilized as a building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its cyclopropane ring imparts remarkable reactivity and stability, making it a valuable intermediate in organic synthesis. Specifically, 2,​2-​Difluorocyclopropane​acetic acid can serve as a key starting material for the synthesis of complex molecules by participating in diverse reactions such as cycloaddition, ring-opening, and functional group transformations. Its fluorinated nature also introduces desirable properties like altered lipophilicity and increased stability in biological systems. In summary, the strategic incorporation of 2,​2-​Difluorocyclopropane​acetic acid in chemical synthesis enables the efficient construction of diverse molecular architectures with potential applications in various industries.