303461
(R)-(+)-β-Citronellol
95%
Sinónimos:
(+)-β-Citronellol, (R)-3,7-Dimethyl-6-octen-1-ol
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Acerca de este artículo
Fórmula lineal:
(CH3)2C=CHCH2CH2CH(CH3)CH2CH2OH
Número CAS:
Peso molecular:
156.27
UNSPSC Code:
12352002
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-250-5
Beilstein/REAXYS Number:
1721506
MDL number:
Assay:
95%
Form:
liquid
Servicio técnico
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Permítanos ayudarlevapor pressure
~0.02 mmHg ( 25 °C)
assay
95%
form
liquid
optical activity
[α]19/D +5.3°, neat
refractive index
n20/D 1.456 (lit.)
bp
112-113 °C/12 mmHg (lit.)
density
0.857 g/mL at 25 °C (lit.)
functional group
hydroxyl
SMILES string
C[C@@H](CCO)CC\C=C(\C)C
InChI
1S/C10H20O/c1-9(2)5-4-6-10(3)7-8-11/h5,10-11H,4,6-8H2,1-3H3/t10-/m1/s1
InChI key
QMVPMAAFGQKVCJ-SNVBAGLBSA-N
Application
(R)-(+)-β-Citronellol can be used to prepare:
It can also be used as a starting material for the synthesis of (+)-integerrinecic acid lactone.
- (R)-(+)-β-citronellyl acetate by treating with vinyl acetate via trans esterification reaction using immobilized Rhizomucor miehei lipase as biocatalyst.
- (R)-(+)-citronellal and (R)-(+)-citronellic acid by the oxidation reaction.
- Citronellol aziridine by treating with 2,2,2-trichloroethoxysulfonamide by intermolecular olefin aziridination.
It can also be used as a starting material for the synthesis of (+)-integerrinecic acid lactone.
(R)-(+)-β-Citronellol can undergo:
- Oxidation to form (R)-(+)-citronellal, an antifungal agent and (R)-(+)-citronellic acid.
- Intermolecular olefin aziridination with 2,2,2-trichloroethoxysulfonamide to form citronellol aziridine for ring-opening reactions.
- Series of reactions to form α2δ-ligands for treating generalized anxiety disorder and insomnia.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Clase de almacenamiento
10 - Combustible liquids
flash_point_f
212.0 °F - closed cup
flash_point_c
100 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Study of the antifungal potential of (r)-(+)-citronellal and its association with therapeutic agents used in the treatment of vulvovaginal candidiasis.
Medeiros CIS, et al.
Bioscience Journal, 33(2), 3041-3043 (2017)
Wuryatmo E
Application of citral to control postharvest diseases of oranges. (2011)
Diastereoselective, large-scale synthesis of ?-amino acids via asymmetric aza-Michael addition as ?2? ligands for the treatment of generalized anxiety disorder and insomnia.
Magano J, et al.
Tetrahedron Letters, 50(46), 6325-6328 (2009)