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272078

(1S)-(+)-Camphorquinone

Name: (1<I>S</I>)-(+)-Camphorquinone
Brand: ALDRICH

99%

Synonym(s):

(1S)-(+)-Bornanedione

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About This Item

Empirical Formula (Hill Notation):

C₁₀H₁₄O₂

CAS Number:

2767-84-2

Molecular Weight:

166.22

UNSPSC Code:

12352115

NACRES:

NA.22

PubChem Substance ID:

24856452

EC Number:

220-446-1

Beilstein/REAXYS Number:

2613999

MDL number:

MFCD00064159

Assay:

99%

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Properties

Quality Level

100

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

Description

Application

Bioreduction of quinones and other ketones by red algae.

Chiral starting material.

wgk

WGK 3

flash_point_f

Not applicable

Storage Class

11 - Combustible Solids

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Comparison between two methods to evaluate temperature changes produced by composite light curing units and polymerization techniques.

F H F Loureiro et al.

Minerva stomatologica, 60(10), 501-508 (2011-11-16)

This study evaluated the temperature change into the pulp chamber during the light curing of composite resin by direct (bovine tooth) and indirect (matrix) methods. Direct method: fifty standardized cavities (2x2x2 mm) were prepared in bovine incisors, which were randomly

Degree of conversion and microhardness of TPO-containing resin-based composites cured by polywave and monowave LED units.

Ario Santini et al.

Journal of dentistry, 40(7), 577-584 (2012-04-03)

To determine the degree of conversion (DC) and Knoop microhardness (KHN) of resin-based composites (RBCs) containing trimethylbenzoyl-diphenylphosphine oxide (TPO) cured by polywave or monowave LED light-curing units (LCUs). Three groups (each n = 5) of Tetric EvoCeram (Ivoclar Vivadent), Vit-l-escence

Excited-state properties of a photochromic spirooxazine: double pathways for both fluorescence emission and camphorquinone-sensitized reaction.

Maria Rosaria di Nunzio et al.

The journal of physical chemistry. A, 113(34), 9424-9433 (2009-08-07)

In this article, we report a study on the singlet and triplet excited-state properties of a spirooxazine (1,3-dihydro-3,3-dimethyl-1-isobutyl-6'-(2,3-dihydro-1H-indol-1-yl)spiro[2H-indole-2,3'-3H-naphtho[2,1-b][1,4]oxazine]). The singlet state of this molecule is photoreactive: upon UV light stimulation, it produces a colored merocyanine that thermally reverts to the

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Global Trade Item Number

SKU	GTIN
272078-5G	04061832718989