Search Thermo Fisher Scientific
Element Search
Structure Search
Thermo Scientific Chemicals
(1R)-(+)-Camphor, 98%, Thermo Scientific Chemicals
Have Questions?
Change view
Catalog number A10708.36
also known as A10708-36
Price (USD)/ Each
158.00
-
Quantity:
500 g
Price (USD)/ Each
158.00
(1R)-(+)-Camphor, 98%, Thermo Scientific Chemicals
Catalog numberA10708.36
Price (USD)/ Each
158.00
-
Chemical Identifiers
CAS464-49-3
IUPAC Name(1R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
Molecular FormulaC10H16O
InChI KeyDSSYKIVIOFKYAU-XVKPBYJWSA-N
SMILESCC1(C)[C@H]2CC[C@@]1(C)C(=O)C2
View more
Specifications
Specification Sheet
Specification SheetAppearance (Color)White
Melting Point (clear melt)174.0-180.0°C
Optical Rotation+41.0 to +45.5° (c=10 in ethanol)
Assay (GC)≥97.5%
FormCrystals or powder or crystalline powder or lumps or fused solid
View more
(1R)-(+)-Camphor is used as a chiral intermediate and auxiliary. It is also used as a skin antipruritic and as an anti-infective agent.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
(1R)-(+)-Camphor is used as a chiral intermediate and auxiliary. It is also used as a skin antipruritic and as an anti-infective agent.
Solubility
Soluble in water (0.1 g/L at 20°C).
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
(1R)-(+)-Camphor is used as a chiral intermediate and auxiliary. It is also used as a skin antipruritic and as an anti-infective agent.
Solubility
Soluble in water (0.1 g/L at 20°C).
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- G. Grogan.; G. Roberts.; S. Parsons, N. Turner.; S. Flitsch. P450camr, a cytochrome P450 catalysing the stereospecific 6-endo-hydroxylation of (1R)-(+)-camphor. Applied Microbiology and Biotechnology. 2002, 59, (4), 449-454.
- V Santhi.; J.Madhusudana Rao. Asymmetric reduction of prochiral ketones using in situ generated oxazaborolidines derived from amino alcohols of (1R)-camphor as catalysts. Tetrahedron: Asymmetry. 2000, 11 (17), 3553-3560.