276286
(1R)-(−)-Camphorquinone
99%
Synonym(s):
(1R)-(−)-2,3-Bornanedione, 2,3-Bornanedione
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| Size/SKU | Availability | Price |
|---|---|---|
5 g | Available to ship TODAY | $258.00 |
About This Item
$258.00
Available to ship TODAYDetails
Quality Segment
assay
99%
optical activity
[α]20/D −101°, c = 2 in toluene
mp
200-203 °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+/m1/s1
InChI key
VNQXSTWCDUXYEZ-LDWIPMOCSA-N
Application
- 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.
1 of 1
This Item | ||
|---|---|---|
| description 99% | description 98% | description analytical standard |
| assay 99% | assay 98% | assay ≥99.0% (sum of enantiomers, GC) |
| Quality Level 100 | Quality Level 100 | Quality Level 100 |
| mp 200-203 °C (lit.) | mp 198 °C (dec.) (lit.) | mp - |
| optical activity [α]20/D −101°, c = 2 in toluene | optical activity [α]20/D −21°, c = 2 in H2O | optical activity [α]20/D -81±1°, c = 8% in benzene |
| functional group ketone | functional group ketone, sulfonic acid | functional group - |
Signal Word
Danger
Hazard Codes
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Resp. Sens. 1
Storage Class
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
PPE (personal protective equipment)
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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