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Sigma-Aldrich

(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

Quality Level

assay

99%

optical activity

[α]20/D +100°, c = 1.9 in toluene

mp

197-201 °C (lit.)

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.

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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Journal of biomedical materials research. Part A, 93(4), 1245-1251 (2009-10-15)
The selection of an appropriate photoinitiator system is critical for efficient polymerization of dental resins with satisfactory mechanical and physical properties. The purpose of this study was to evaluate the influence of adding an iodonium salt to two-component photoinitiator systems.
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