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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,2S,4R)-

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,2S,4R)-
CAS Number: 20347-65-3
Product Number: AG0028X0(AGN-PC-0O7AYL)
Synonyms:
MDL No:
Molecular Formula: C12H20O2
Molecular Weight: 196.2860

Identification/Properties

Properties
BP:
223.5°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Refractive Index:
n20/D 1.463
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:
196.146g/mol
Monoisotopic Mass:
196.146g/mol
Topological Polar Surface Area:
26.3A^2
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, (+)-Bornyl acetate plays a crucial role as a versatile building block. This compound, derived from natural sources such as essential oils, serves as a valuable precursor in the creation of various synthetic molecules and materials. (+)-Bornyl acetate is commonly utilized as a chiral starting material due to its unique stereochemistry, allowing chemists to introduce specific chirality into their target molecules. Through strategic functional group transformations and manipulation of its structure, chemists can easily access a wide range of complex organic compounds by utilizing (+)-Bornyl acetate as a key intermediate. This compound's utility in chemical synthesis extends to the fields of pharmaceuticals, fragrances, and materials science, where its incorporation enables efficient access to structurally diverse and biologically active compounds.