Myrtenal

Base Information

Chemical Name:Myrtenal
CAS No.:564-94-3
Molecular Formula:C10H14 O
Molecular Weight:150.221
Hs Code.:
European Community (EC) Number:209-274-8
NSC Number:54384
DSSTox Substance ID:DTXSID60865112
Nikkaji Number:J121.133A
Wikipedia:Myrtenal
Wikidata:Q104253270
Metabolomics Workbench ID:28175
Mol file:564-94-3.mol

Synonyms:myrtenal

Suppliers and Price of Myrtenal

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
Myrtenal(MixtureofEnantiomers)
250mg
$ 50.00

Total 30 raw suppliers

Chemical Property of Myrtenal

Chemical Property:

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
Storage Temp.:2-8°C
Solubility.:Chloroform (Sparingly), Methanol (Slightly)
XLogP3:2.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:150.104465066
Heavy Atom Count:11
Complexity:225

Purity/Quality:

97% ^*data from raw suppliers

Myrtenal(MixtureofEnantiomers) ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 23-24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CC1(C2CC=C(C1C2)C=O)C
Description 2-Formyl-6,6-dimethylbicyclo(3.1.1 -)hept-2-ene has a refreshing, spicy-herbaceous odor of bay leaf, reminiscent of cinnamon. This substance may be synthesized from myrtenol by oxidation with chromic acid; by isolation from higher-than-cineole boiling fractions in the distillation of eucalyptus oil.

Technology Process of Myrtenal

There total 62 articles about Myrtenal which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 98.0%

: 19894-97-4
(1R)-Myrtenol

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

Guidance literature:: With fluorosulfonyl fluoride; potassium carbonate; dimethyl sulfoxide; at 20 ℃; for 12h; chemoselective reaction;
DOI:10.1002/adsc.201900104

Reference yield: 58.0%

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

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

Guidance literature:: With pyridine; dmap; 5,10,15,20-tetrakisphenylporphyrin; oxygen; acetic anhydride; In dichloromethane; for 2.5h; Irradiation;
DOI:10.1021/jo00170a060