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(-)-MYRTENOL

  • Product Name (-)-MYRTENOL
  • cas 19894-97-4
  • purity 99%
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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

(1R)-6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-methanol-10-O-α-D-apiofuranosyl-(1→6)-β-D-glucopyranoside

D-apiose
639-97-4,6477-44-7,42927-70-8

D-apiose

D-glucose
50-99-7

D-glucose

(1R)-Myrtenol
19894-97-4

(1R)-Myrtenol

Conditions
Conditions Yield
With hydrogenchloride; water; at 90 ℃; for 2h;
formaldehyd
50-00-0,30525-89-4,61233-19-0

formaldehyd

beta-pinene
18172-67-3,19902-08-0,25719-60-2

beta-pinene

pinocarvone
34413-88-2

pinocarvone

myrtenal
564-94-3,18486-69-6

myrtenal

trans-pinocarveol
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

nopadiene
30293-06-2

nopadiene

(1R)-(-)-nopol
35836-73-8

(1R)-(-)-nopol

(1R)-Myrtenol
19894-97-4

(1R)-Myrtenol

Conditions
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
    80-56-8

    rac-α-pinene

  • 127-91-3
    127-91-3

    (1R/S,5R/S)-6,6-dimethyl-2-methylenebicyclo[3.1.1]heptane

  • 564-94-3
    564-94-3

    (+/-)-(1S,5R)-6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

  • 56246-58-3
    56246-58-3

    β-pinene oxide

19894-97-4 Downstream products

  • 17066-59-0
    17066-59-0

    (+/-)-O -(2-Carboxy-benzoyl)-myrtenol

  • 473-01-8
    473-01-8

    trans-myrtanol

  • 473-01-8
    473-01-8

    ((1S*,2R*,5S*)-6,6-dimethylbicyclo[3.1.1]heptan-2-yl)methanol

  • 564-94-3
    564-94-3

    (+/-)-(1S,5R)-6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

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