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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)-

1,3-bis(1-adamantyl)imidazolidin-1-ium;tetrafluoroborate

C1C2CC3CC1CC(C2)(C3)N1CC[NH+](C1)C12CC3CC(C2)CC(C1)C3.F[B-](F)(F)F Request for Quotation
Chemical Name: 1,3-bis(1-adamantyl)imidazolidin-1-ium;tetrafluoroborate
CAS Number: 1176202-63-3
Product Number: AG008VFB(AGN-PC-0BKEAZ)
Synonyms:
MDL No:
Molecular Formula: C23H37BF4N2
Molecular Weight: 428.3579

Identification/Properties

Computed Properties
Molecular Weight:
428.367g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
428.299g/mol
Monoisotopic Mass:
428.299g/mol
Topological Polar Surface Area:
7.7A^2
Heavy Atom Count:
30
Formal Charge:
0
Complexity:
517
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:
Danger
UN#:
1759
Hazard Statements:
H302-H314
Precautionary Statements:
P501-P260-P270-P264-P280-P303+P361+P353-P301+P330+P331-P363-P301+P312+P330-P304+P340+P310-P305+P351+P338+P310-P405
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,3-Di(1-adamantyl)imidazolinium Tetrafluoroborate is a versatile catalyst widely used in chemical synthesis reactions. Its unique structure imparts exceptional catalytic properties, making it highly effective in promoting a variety of organic transformations. This catalyst has found particular success in asymmetric catalysis, facilitating enantioselective reactions with high efficiency and selectivity. Additionally, 1,3-Di(1-adamantyl)imidazolinium Tetrafluoroborate has been utilized in the synthesis of complex natural products and pharmaceutical compounds, showcasing its remarkable utility in the field of organic chemistry. Its robust catalytic activity and compatibility with a wide range of substrates make it a valuable tool for researchers and synthetic chemists seeking to streamline their synthetic pathways and access challenging molecular motifs.