272078
(1S)-(+)-Camphorquinone
99%
Synonym(s):
(1S)-(+)-Bornanedione
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About This Item
Empirical Formula (Hill Notation):
C10H14O2
CAS Number:
Molecular Weight:
166.22
Beilstein/REAXYS Number:
2613999
EC Number:
MDL number:
UNSPSC Code:
12352115
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
99%
optical activity
[α]20/D +100°, c = 1.9 in toluene
mp
197-201 °C (lit.)
functional group
ketone
SMILES string
CC1(C)[C@H]2CC[C@]1(C)C(=O)C2=O
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
InChI key
VNQXSTWCDUXYEZ-QUBYGPBYSA-N
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Application
Bioreduction of quinones and other ketones by red algae.
Chiral starting material.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Ettore Castiglioni et al.
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Among the various chiroptical spectroscopic techniques available today, circularly polarized luminescence (CPL) plays a minor role and is still used by a limited number of specialists. The cost of the few commercial instruments available and the complexity of homemade apparatuses
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This paper reviews our recent studies on radical photopolymerization initiators, which are used in the design of light-curing dental adhesives and resin composites, by collating information of related studies from original scientific papers, reviews, and patent literature. The photopolymerization reactivities
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F H F Loureiro et al.
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