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(1R)-(+)-Alcanfor, 98 %, Thermo Scientific Chemicals

Thermo Scientific Chemicals

(1R)-(+)-Alcanfor, 98 %, Thermo Scientific Chemicals

Name: (1R)-(+)-Alcanfor, 98 %, Thermo Scientific Chemicals
SKU: A10708.14
Price: 26.50 EUR

CAS: 464-49-3 | C10H16O | 152.24 g/mol

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25 g

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Número de catálogo A10708.14

también denominado A10708-14

Precio (EUR)

26,50

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Cantidad:

25 g

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Precio (EUR)

26,50

Each

Identificadores químicos

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

Especificaciones Specification Sheet

Hoja de especificaciones

Appearance (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%

Identification (FTIR)Conforms

(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.

Aplicaciones
El (1R)-(+)-alcanfor se usa como un intermedio quiral y auxiliar. También se utiliza como antiprurítico de la piel y como agente antiinfeccioso.

Solubilidad
Soluble en agua (0,1 g/l a 20 °C).

Notas
Mantener el recipiente bien sellado. Almacenar en un lugar fresco y seco y en recipientes bien sellados. Incompatible con agentes oxidantes.

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.