- Product Name (-)-MYRTENOL
- cas 19894-97-4
- purity 99%
Reputable supplier selling (-)-MYRTENOL 19894-97-4 with stock
- Molecular Formula: C10H16 O
- Molecular Weight: 152.236
- Appearance/Colour: colorless liquid
- Refractive Index: n20/D 1.496
- Boiling Point: 221-222 °C(lit.)
- PKA: 14.77±0.10(Predicted)
- Flash Point: 193 °F
- PSA: 20.23000
- Density: 0.981 g/mL at 20 °C(lit.)
- LogP: 1.97110
(-)-MYRTENOL(Cas 19894-97-4) Usage
|
General Description |
(?)-Myrtenol is a naturally occurring monoterpene alcohol, belonging to the class of volatile organic compounds. It is widely used in fragrance, cosmetic products, cleaning agents and flavoring agents in a variety of food products. |
InChI:InChI=1/C10H16O/c1-10(2)8-4-3-7(6-11)9(10)5-8/h3,8-9,11H,4-6H2,1-2H3/t8?,9-/m0/s1
19894-97-4 Relevant articles
New inhibitors of tyrosyl-DNA phosphodiesterase I (Tdp 1) combining 7-hydroxycoumarin and monoterpenoid moieties
Khomenko, Tatyana,Zakharenko, Alexandra,Odarchenko, Tatyana,Arabshahi, Homayon John,Sannikova, Victoriya,Zakharova, Olga,Korchagina, Dina,Reynisson, Jóhannes,Volcho, Konstantin,Salakhutdinov, Nariman,Lavrik, Olga
, p. 5573 - 5581 (2016)
A number of derivatives of 7-hydroxycoum...
New monoterpene glycosides from sunflower seeds and their protective effects against H2O2-induced myocardial cell injury
Fei, Yonghe,Zhao, Jianping,Liu, Yanli,Li, Xiaoran,Xu, Qiongming,Wang, Taoyun,Khan, Ikhlas A.,Yang, Shilin
, p. 385 - 390 (2015)
Three new monoterpene glycosides (1-3) a...
-
Zweifel,G.,Whitney,C.C.
, p. 4178 - 4180 (1966)
-
Molecular Chirality and Cloud Activation Potentials of Dimeric α-Pinene Oxidation Products
Bé, Ariana Gray,Bellcross, Aleia,Geiger, Franz M.,Thomson, Regan J.
supporting information, p. 16653 - 16662 (2021/10/20)
The surface activity of ten atmospherica...
New hybrid compounds combining fragments of usnic acid and monoterpenoids for effective tyrosyl-dna phosphodiesterase 1 inhibition
Dyrkheeva, Nadezhda S.,Filimonov, Aleksandr S.,Luzina, Olga A.,Zakharenko, Alexandra L.,Ilina, Ekaterina S.,Malakhova, Anastasia A.,Medvedev, Sergey P.,Reynisson, Jóhannes,Volcho, Konstantin P.,Zakian, Suren M.,Salakhutdinov, Nariman F.,Lavrik, Olga I.
, (2021/07/02)
Usnic acid (UA) is a secondary metabolit...
Selective C-H Allylic Oxygenation of Cycloalkenes and Terpenoids Photosensitized by [Cu(Xantphos)(neoc)]BF4
Kallitsakis, Michael G.,Gioftsidou, Dimitra K.,Tzani, Marina A.,Angaridis, Panagiotis A.,Terzidis, Michael A.,Lykakis, Ioannis N.
, p. 13503 - 13513 (2021/09/13)
We present herein for the first time the...
Deep eutectic solvents as H2-sources for Ru(II)-catalyzed transfer hydrogenation of carbonyl compounds under mild conditions
Cavallo, Marzia,Arnodo, Davide,Mannu, Alberto,Blangetti, Marco,Prandi, Cristina,Baratta, Walter,Baldino, Salvatore
supporting information, (2021/02/22)
The employment of easily affordable ruth...
19894-97-4 Process route
-
-
(1R)-6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-methanol-10-O-α-D-apiofuranosyl-(1→6)-β-D-glucopyranoside
-
-
639-97-4,6477-44-7,42927-70-8
D-apiose
-
-
50-99-7
D-glucose
-
-
19894-97-4
(1R)-Myrtenol
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride; water;
at 90 ℃;
for 2h;
|
-
-
50-00-0,30525-89-4,61233-19-0
formaldehyd
-
-
18172-67-3,19902-08-0,25719-60-2
beta-pinene
-
-
34413-88-2
pinocarvone
-
-
564-94-3,18486-69-6
myrtenal
-
-
547-61-5,1674-08-4,2158-49-8,3917-59-7,5947-36-4,6712-79-4,19889-99-7,19894-98-5
trans-pinocarveol
-
-
30293-06-2
nopadiene
-
-
35836-73-8
(1R)-(-)-nopol
-
-
19894-97-4
(1R)-Myrtenol
| Conditions | Yield |
|---|---|
|
With
sulfated zinc ferrite;
In
toluene;
at 95 ℃;
for 12h;
Reagent/catalyst;
Temperature;
Concentration;
Solvent;
|
19894-97-4 Upstream products
-
80-56-8
rac-α-pinene
-
127-91-3
(1R/S,5R/S)-6,6-dimethyl-2-methylenebicyclo[3.1.1]heptane
-
564-94-3
(+/-)-(1S,5R)-6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
-
56246-58-3
β-pinene oxide
19894-97-4 Downstream products
-
17066-59-0
(+/-)-O -(2-Carboxy-benzoyl)-myrtenol
-
473-01-8
trans-myrtanol
-
473-01-8
((1S*,2R*,5S*)-6,6-dimethylbicyclo[3.1.1]heptan-2-yl)methanol
-
564-94-3
(+/-)-(1S,5R)-6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde