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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-ol, 1,7,7-trimethyl-, acetate, (1R,2R,4R)-rel-

CC(=O)O[C@@H]1C[C@@H]2C([C@@]1(C)CC2)(C)C Request for Quotation
Chemical Name: Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, acetate, (1R,2R,4R)-rel-
CAS Number: 125-12-2
Product Number: AG000MYO(AGN-PC-0PHYPU)
Synonyms:
MDL No:
Molecular Formula: C12H20O2
Molecular Weight: 196.2860

Identification/Properties

Computed Properties
Molecular Weight:
196.29g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
196.14633g/mol
Monoisotopic Mass:
196.14633g/mol
Topological Polar Surface Area:
26.3Ų
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
270
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
3
Undefined Atom Stereocenter Count:
0
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:
Warning
UN#:
-
Hazard Statements:
H227-H316
Precautionary Statements:
P210-P280-P332+P313-P370+P378-P403+P235-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound rel-(1R,2R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl acetate has a significant application in chemical synthesis as a versatile building block. Its unique structure and reactivity make it a valuable intermediate for the construction of complex organic molecules. Specifically, this compound can be used as a chiral source in asymmetric synthesis, enabling the creation of enantiomerically pure compounds. In addition, its bicycle framework offers the opportunity for diverse functional group manipulations, allowing for the creation of a variety of structurally diverse compounds. This compound plays a crucial role in the construction of biologically active molecules, pharmaceuticals, and fine chemicals due to its ability to introduce chirality and complexity with high efficiency.