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(R)-(−)-Carvone

ALDRICH/124931 - 98%

Synonym: (−)-Carvone; (R)-5-Isopropenyl-2-methyl-2-cyclohexenone; p-Mentha-6,8-dien-2-one; Carvol

CAS Number: 6485-40-1
Empirical Formula (Hill Notation): C10H14O
Molecular Weight: 150.22
EC Number: 229-352-5
MDL Number: MFCD00001578
Linear Formula: C10H14O
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-124931-5ML 5 mL
 $0.00
1/EA
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45-124931-100ML 100 mL
 $69.30
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45-124931-500ML 500 mL
 $158.00
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assay 98%
bp 227-230 °C (lit.)
density 0.959 g/mL at 25 °C (lit.)
form liquid
functional group ketone
InChI 1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3/t9-/m1/s1
InChI key ULDHMXUKGWMISQ-SECBINFHSA-N
optical activity [α]20/D −61°, neat
Quality Level 100 
refractive index n20/D 1.497 (lit.)
SMILES string CC(=C)[C@@H]1CC=C(C)C(=O)C1
vapor density 5.2 (vs air)
vapor pressure 0.4 mmHg ( 20 °C)
Application: (R)-(−)-Carvone may be employed as starting reagent for the synthesis of enantiopure (R)-(+)-3-methyl-6-isopropenyl-cyclohept-3-enone-1, a useful intermediate formed during the synthesis of terpenoids. It may be employed as starting reagent for the synthesis of differently protected (4S,6R,7R)-trihydroxy-1-octyne derivatives.
Application: Chiral starting material.
General description: (R)-(−)-Carvone is a monoterpenoid. Its ozonolysis in the gaseous phase has been proposed. Aldehydes (formaldehyde) and biradicals were obtained as the major products. It participates in the diastereoselective synthesis of homochiral octalones.
Packaging: 100, 500 mL in poly bottle
Packaging: 5 mL in glass bottle
Purity 98%
bp 227-230 °C (lit.)
Density 0.959 g/mL at 25 °C (lit.)
Refractive Index n20/D 1.497 (lit.)
UNSPSC 12352115

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