| Identification | More | [Name]
(1S)-(+)-CAMPHORQUINONE | [CAS]
2767-84-2 | [Synonyms]
(1S)-(+)-2,3-BORNANEDIONE
(1S)-2,3-BORNANEDIONE
(1S,4R)-1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPTANE-2,3-DIONE
(1S)-(+)-BORNANEDIONE
(1S)-(+)-CAMPHORQUINONE
(+)-2,3-BORNANEDIONE
(+)-CAMPHORQUINONE
CAMPHORQUINONE,-S-(+)-
L-2, 3-BORNANEDIONE
L-(+)-CAMPHORQUINONE
L-CAMPHORQUINONE
S-(+)-CAMPHORQUINONE
3-dione,1,7,7-trimethyl-,(1S)-Bicyclo[2.2.1]heptane-2
7,7-trimethyl-3-dion(1s)-bicyclo[2.2.1]heptane-1
(1S)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione
Bicyclo2.2.1heptane-2,3-dione, 1,7,7-trimethyl-, (1S,4R)-
(1S,4β)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione | [EINECS(EC#)]
220-446-1 | [Molecular Formula]
C10H14O2 | [MDL Number]
MFCD00064159 | [Molecular Weight]
166.22 | [MOL File]
2767-84-2.mol |
| Chemical Properties | Back Directory | [Appearance]
YELLOW POWDER | [Melting point ]
197-201 °C(lit.) | [alpha ]
+100° (20/D)(c=1.9, C6H5CH3) | [Boiling point ]
234.44°C (rough estimate) | [density ]
0.9817 (rough estimate) | [refractive index ]
1.4859 (estimate) | [form ]
powder to crystal | [color ]
White to Yellow to Orange | [Optical Rotation]
[α]20/D +100°, c = 1.9 in toluene | [BRN ]
2613999 | [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 | [InChIKey]
VNQXSTWCDUXYEZ-QUBYGPBYSA-N | [SMILES]
CC1(C)[C@H]2CC[C@]1(C)C(=O)C2=O | [CAS DataBase Reference]
2767-84-2(CAS DataBase Reference) | [EPA Substance Registry System]
Bicyclo[2.2.1]heptane-2,3-dione, 1,7,7-trimethyl-, (1S,4R)- (2767-84-2) |
| Safety Data | Back Directory | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [F ]
10 | [TSCA ]
Yes | [HS Code ]
29142900 | [Storage Class]
11 - Combustible Solids |
| Hazard Information | Back Directory | [Chemical Properties]
YELLOW POWDER | [Uses]
Chiral starting material. | [Definition]
ChEBI: (1S)-bornane-2,3-dione is a bornane-2,3-dione. It is an enantiomer of a (1R)-bornane-2,3-dione. | [Purification Methods]
It can be purified by steam distillation, recrystallisation (yellow prisms) from EtOH, *C6H6 or Et2O/pet ether and it can be sublimed in a vacuum. The (±)-quinone forms needles from EtOH, m 197-198o, 203o. [Buxtorf & Flatt Helv Chim Acta 13 1026 1930, Asahena et al. Chem Ber 67 1432 1934, Beiltein 7 I 325.] |
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