(1R)-(-)-Camphorquinone

Base Information Edit

Chemical Name:(1R)-(-)-Camphorquinone
CAS No.:10334-26-6
Deprecated CAS:465-29-2
Molecular Formula:C10H14O2
Molecular Weight:166.22
Hs Code.:2914299000
European Community (EC) Number:626-988-9
UNII:RAL3591W33
Nikkaji Number:J232.216A
Wikidata:Q27116959
Metabolomics Workbench ID:28182
Mol file:10334-26-6.mol

Synonyms:camphorquinone

Suppliers and Price of (1R)-(-)-Camphorquinone

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
(1R)-(-)Camphorquinone
1g
$ 140.00

TCI Chemical
(1R)-(-)-Camphorquinone >98.0%(GC)
1g
$ 33.00

TCI Chemical
(1R)-(-)-Camphorquinone >98.0%(GC)
5g
$ 96.00

Sigma-Aldrich
(1R)-(?)-Camphorquinone 99%
5g
$ 111.00

Sigma-Aldrich
(1R)-(?)-Camphorquinone analytical standard
50mg
$ 49.30

Crysdot
(1R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione 95+%
100g
$ 633.00

Chem-Impex
(1R)-(-)-Camphorquinon,98%(GC) 98%(GC)
1G
$ 31.36

Chem-Impex
(1R)-(-)-Camphorquinon,98%(GC) 98%(GC)
5G
$ 100.80

Biosynth Carbosynth
(1R)-(-)-Camphorquinone
2 g
$ 90.00

Biosynth Carbosynth
(1R)-(-)-Camphorquinone
1 g
$ 50.00

Total 34 raw suppliers

Chemical Property of (1R)-(-)-Camphorquinone Edit

Chemical Property:

Vapor Pressure:0.0817mmHg at 25°C
Melting Point:200-203 °C(lit.)
Refractive Index:1.5
Boiling Point:226.473 °C at 760 mmHg
Flash Point:82.965 °C
PSA：34.14000
Density:1.098 g/cm³
LogP:1.58070
Storage Temp.:Store below +30°C.
Solubility.:almost transparency in Methanol
XLogP3:1.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:166.099379685
Heavy Atom Count:12
Complexity:278

Purity/Quality:

98%,99%, ^*data from raw suppliers

(1R)-(-)Camphorquinone ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn
Hazard Codes:Xn
Statements: 22-43
Safety Statements: 36/37

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(C2CCC1(C(=O)C2=O)C)C
Isomeric SMILES:C[C@@]12CC[C@@H](C1(C)C)C(=O)C2=O
Uses (1R)-(-)Camphorquinone are used as visible light photoinitiator for biomedical applications such as in dental surgery. (1R)-(?)-Camphorquinone can be used as a chiral starting material for the preparation of: α-Hydroxycamphors by selective reduction of keto groups using various vegetables. Camphor-1,2-diamine platinum(II) complexes for DNA interaction studies. Camphoric anhydride by unsensitized photo-oxidation in the presence of oxygen and polar solvents. Camphorquinone-based chiral homoallylic amine, which is reacted with aldehydes to produce homoallylic primary amines via imine formation followed by 2-azonia-Cope rearrangement. (1R)-(-)-Camphorquinone may be used as an analytical standard for the determination of the analyte in dental resin composite restorations in the oral environment in contact with food and beverages, and biological samples by analytical techniques.

Technology Process of (1R)-(-)-Camphorquinone

There total 122 articles about (1R)-(-)-Camphorquinone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 98.0%