(1S)-(+)-Camphorquinone

The Bicyclo[2.2.1]heptane-2,3-dione,1,7,7-trimethyl-, (1S,4R)- with CAS registry number of 2767-84-2 is also known as (1S)-(+)-Camphorquinone. The Systematic name is (1S,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione. It belongs to product categories of Bicyclic Monoterpenes; Biochemistry; Terpenes; Ring Systems. Its EINECS registry number is 220-446-1. In addition, the formula is C₁₀H₁₄O₂ and the molecular weight is 166.22. This chemical is a yellow powder and should be sealed in cool, dry place. During using it, do not breathe dust and avoid contact with skin or eyes.

Physical properties about Bicyclo[2.2.1]heptane-2,3-dione,1,7,7-trimethyl-, (1S,4R)- are: (1)ACD/LogP: 1.47; (2)ACD/LogD (pH 5.5): 1.47; (3)ACD/LogD (pH 7.4): 1.47; (4)ACD/BCF (pH 5.5): 7.75; (5)ACD/BCF (pH 7.4): 7.75; (6)ACD/KOC (pH 5.5): 150.76; (7)ACD/KOC (pH 7.4): 150.76; (8)#H bond acceptors: 2; (9)Index of Refraction: 1.5; (10)Molar Refractivity: 44.52 cm³; (11)Molar Volume: 151.3 cm³; (12)Surface Tension: 36.6 dyne/cm; (13)Density: 1.098 g/cm³; (14)Flash Point: 83 °C; (15)Enthalpy of Vaporization: 46.3 kJ/mol; (16)Boiling Point: 226.5 °C at 760 mmHg; (17)Vapour Pressure: 0.0817 mmHg at 25 °C.

Uses of Bicyclo[2.2.1]heptane-2,3-dione,1,7,7-trimethyl-, (1S,4R)-: it is used to produce 3-hydroxy-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-one and 3-hydroxy-4,7,7-trimethyl-bicyclo[2.2.1]heptan-2-one. The reaction occurs with reagents In, NH₄Cl and solvent methanol, H₂O with other condition of heating. The yield is about 50%.

You can still convert the following datas into molecular structure:
1. SMILES: O=C1C(=O)[C@@H]2CC[C@@]1(C)C2(C)C
2. InChI: InChI=1/C10H14O2/c1-9(2)6-4-5-10(9,3)8(12)7(6)11/h6H,4-5H2,1-3H3/t6-,10+/m0/s1
3. InChIKey: VNQXSTWCDUXYEZ-QUBYGPBYBK
4. Std. InChI: InChI=1S/C10H14O2/c1-9(2)6-4-5-10(9,3)8(12)7(6)11/h6H,4-5H2,1-3H3/t6-,10+/m0/s1
5. Std. InChIKey: VNQXSTWCDUXYEZ-QUBYGPBYSA-N