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  2. Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, oxime, (1R,4R)-

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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)-

Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, oxime, (1R,4R)-

O/N=C/1C[C@@H]2C([C@@]1(C)CC2)(C)C Request for Quotation
Chemical Name: Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, oxime, (1R,4R)-
CAS Number: 2792-42-9
Product Number: AG003BFW(AGN-PC-0O8JF3)
Synonyms:
MDL No:
Molecular Formula: C10H17NO
Molecular Weight: 167.2481

Identification/Properties

Properties
MP:
115-119℃
BP:
242.983°C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
167.252g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
167.131g/mol
Monoisotopic Mass:
167.131g/mol
Topological Polar Surface Area:
32.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
244
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The oxime of (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one serves as a versatile tool in chemical synthesis. This compound finds application as a valuable intermediate in various organic reactions, particularly in the formation of cyclic compounds. Due to its unique structural properties, (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one oxime can participate in transformations that lead to the generation of complex molecular scaffolds with high stereochemical control. Its ability to undergo selective functional group manipulations makes it a valuable building block for the synthesis of natural products and pharmaceutical agents.