276286
(1R)-(−)-Camphorquinone
99%
Manufacturer: Sigma Aldrich
CAS Number: 10334-26-6
Synonym(S): (1R)-(−)-2,3-Bornanedione, 2,3-Bornanedione
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 5 G | 276286-5-G | In Stock | ₹ 16,832.88 |
276286 - 5 G
In Stock
Quantity
1
Base Price: ₹ 16,832.88
GST (18%): ₹ 3,029.918
Total Price: ₹ 19,862.798
Quality Level
100
Assay
99%
optical activity
[α]20/D −101°, c = 2 in toluene
mp
200-203 °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+/m1/s1
InChI key
VNQXSTWCDUXYEZ-LDWIPMOCSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | (1R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione | -- | ₹ 10,352.76 | |
| | 10334-26-6 | (1R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione | -- | ₹ 1,283.40 - ₹ 20,448.84 |
Related Products
Description
- Application: (1R)-(−)-Camphorquinone can be used as a chiral starting material for the preparation of: α-Hydroxycamphors by selective reduction of keto groups using various vegetables.[1] Camphor-1,2-diamine platinum(II) complexes for DNA interaction studies.[2] Camphoric anhydride by unsensitized photo-oxidation in the presence of oxygen and polar solvents.[3] Camphorquinone-based chiral homoallylic amine, which is reacted with aldehydes to produce homoallylic primary amines via imine formation followed by 2-azonia-Cope rearrangement.[4]
SAFETY INFORMATION
Pictograms
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Resp. Sens. 1
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves