(-)-MYRTENAL
Contact usGood factory exports good (-)-MYRTENAL 564-94-3
- Molecular Formula: C10H14 O
- Molecular Weight: 150.221
- Vapor Pressure: 0.145mmHg at 25°C
- Melting Point: 53-54 °C
- Refractive Index: n20/D 1.504
- Boiling Point: 215.7°Cat760mmHg
- Flash Point: 78.9°C
- PSA: 17.07000
- Density: 1.061g/cm3
- LogP: 2.17770
(-)-MYRTENAL(Cas 564-94-3) Usage
|
Preparation |
From myrtenol by oxidation with chromic acid; by isolation from higher-than-cineole boiling fractions in the distillation of eucalyptus oil. |
|
Taste threshold values |
Taste characteristics at 30 ppm: woody, piney, minty, green cooling, slightly powdery and spicy. |
InChI:InChI=1/C10H14O/c1-10(2)8-4-3-7(6-11)9(10)5-8/h3,6,8-9H,4-5H2,1-2H3/t8-,9-/m0/s1
564-94-3 Relevant articles
Aspect Cinetique des Substitutions Homolytiques Intramoleculaires. Decomposition de Peroxydes Insatures Derives du Pinane
Montaudon, Evelyne,Bourgeois, Marie-Josephe
, p. 9335 - 9342 (1994)
The decomposition, in dichloromethane, o...
Synthesis method of myrtenyl dihydrazide compound with fungal inhibition activity
-
Paragraph 0046; 0049-0050, (2021/07/17)
A synthesis method of a myrtenyl dihydra...
Synthesis of Myrtenal-Based Nanocellulose/Diacylhydrazine Complexes with Antifungal Activity for Plant Protection
Cen, Bo,Duan, Wengui,Li, Baoyu,Lin, Guishan,Wang, Xiaoyu
, p. 12956 - 12965 (2021/11/17)
In search of novel bioactive compounds w...
Monoterpene-containing substituted coumarins as inhibitors of respiratory syncytial virus (Rsv) replication
Borisevich, Sophia S.,Galochkina, Anastasia V.,Khomenko, Tatyana M.,Korchagina, Dina V.,Nikolaeva, Yulia V.,Petukhova, Galina D.,Salakhutdinov, Nariman F.,Shtro, Anna A.,Volcho, Konstantin P.
, (2021/12/24)
Respiratory syncytial virus (RSV) is a c...
Selective Allylic Oxidation of Terpenic Olefins Using Co-Ag Supported on SiO2 as a Novel, Efficient, and Recyclable Catalyst
Aberkouks, Abderrazak,Mekkaoui, Ayoub Abdelkader,Ait Ali, Mustapha,El Firdoussi, Larbi,El Houssame, Soufiane
, (2020/02/15)
Co-Ag supported on the SiO2 catalyst was...
564-94-3 Process route
-
-
80-56-8,177698-18-9,25766-18-1
Pinene
-
-
80-57-9
verbenone
-
-
1820-09-3,1845-30-3,5416-53-5,13040-03-4,18881-04-4,19890-02-9,22339-08-8,80795-83-1,473-67-6
Verbenol
-
-
515-00-4
myrtenol
-
-
564-94-3
6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
| Conditions | Yield |
|---|---|
|
With
oxygen; rose bengal;
In
N,N-dimethyl-formamide;
at 20 ℃;
for 4h;
UV-irradiation;
|
|
|
With
dihydrogen peroxide;
In
acetonitrile;
at 60 ℃;
for 24h;
Temperature;
|
41 %Chromat.
17 %Chromat. 11 %Chromat. 13 %Chromat. |
-
-
80-56-8,177698-18-9,25766-18-1
Pinene
-
-
80-57-9
verbenone
-
-
1820-09-3,1845-30-3,5416-53-5,13040-03-4,18881-04-4,19890-02-9,22339-08-8,80795-83-1,473-67-6
Verbenol
-
-
564-94-3
6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
| Conditions | Yield |
|---|---|
|
With
2,6-dimethylpyridine; oxygen; rose bengal; acetic anhydride;
In
methanol;
at 20 ℃;
for 4h;
UV-irradiation;
|
564-94-3 Upstream products
-
7785-26-4
(-)-α-pinene
-
18172-67-3
beta-pinene
-
19894-97-4
(1R)-Myrtenol
-
80-56-8
Pinene
564-94-3 Downstream products
-
51152-12-6
(-)-cis-myrtanol
-
2111-71-9
myrtenal
-
71606-83-2
(1R )-pin-2-en-10-al-(2,4-dinitro-phenylhydrazone)
-
49751-95-3
(1R)-10-epi-phenylmyrtenol
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