추천 제품
Quality Level
분석
≥95.0% (sum of enantiomers, GC)
광학 활성
[α]20/D −18±3°, neat
refractive index
n20/D 1.4615 (lit.)
n20/D 1.462
bp
198 °C (lit.)
density
0.862 g/mL at 20 °C (lit.)
작용기
hydroxyl
SMILES string
C\C(C)=C\CC[C@@](C)(O)C=C
InChI
1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3/t10-/m0/s1
InChI key
CDOSHBSSFJOMGT-JTQLQIEISA-N
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일반 설명
(-)-Linalool is a monoterpene compound mainly found in many essential oils. It shows anti-nociceptive and anti-inflammatory activity.
애플리케이션
(-)-Linalool can be used as a reactant in:
- The enantioselective preparation of ophiobolin sesterterpene via diastereoselective reductive radical cascade cyclization.
- The total synthesis of (-)-5,6-dihydrocineromycin B via (-)-linalool O-triethylsilyl ether.;
- The total synthesis of pladienolide B analog.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
166.3 °F - closed cup
Flash Point (°C)
74.6 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
Synthesis of a pladienolide B analogue with the fully functionalized core structure
Organic Letters, 13(15), 3940-3943 (2011)
Phytomedicine : international journal of phytotherapy and phytopharmacology, 23(14), 1727-1734 (2016-12-04)
Essential oil from Cananga odorata (ylang-ylang essential oil, YYO) is usually used in reducing blood pressure, improving cognitive functioning in aromatherapy in human. Few reports showed its effect on anxiety behaviors. To investigate the anxiolytic effects of YYO exposure on
Plant signaling & behavior, 8(1), e22704-e22704 (2012-12-12)
Natural selection is thought to have shaped the evolution of floral scent; however, unlike other floral characters, we have a rudimentary knowledge of how phenotypic selection acts on scent. We found that floral scent was under stronger selection than corolla
(-)-Linalool produces antinociception in two experimental models of pain.
European Journal of Pharmacology, 460(1), 37-41 (2003)
Enantioselective synthesis of an ophiobolin sesterterpene via a programmed radical cascade
Science (New York, N.Y.), 352(6289), 1078-1082 (2016)
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