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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)-

Potassium Chloromethyltrifluoroborate

F[B-](CCl)(F)F.[K+] Request for Quotation
Chemical Name: Potassium Chloromethyltrifluoroborate
CAS Number: 1279123-64-6
Product Number: AG000XK8(AGN-PC-0WALWT)
Synonyms:
MDL No:
Molecular Formula: CH2BClF3K
Molecular Weight: 156.3841

Identification/Properties

Properties
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
156.381g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
155.953g/mol
Monoisotopic Mass:
155.953g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
44.7
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Borate(1-),(chloromethyl)trifluoro-,potassium is a versatile compound widely used in chemical synthesis as a key building block for various reactions. Its unique structure and reactivity make it a valuable reagent in organic chemistry, particularly in the formation of C–C and C–N bonds. This compound serves as a powerful nucleophile and electrophile, enabling efficient transformations in the laboratory. In addition, Borate(1-),(chloromethyl)trifluoro-,potassium is known for its ability to introduce trifluoromethyl groups into organic molecules, making it a valuable tool for the synthesis of fluorinated compounds with diverse applications in pharmaceuticals, agrochemicals, and materials science. Its compatibility with a wide range of functional groups and reaction conditions further enhances its utility in synthetic chemistry, making it a valuable asset for researchers and practitioners seeking to access novel molecules and develop innovative synthetic strategies.