Citreomontanine

Base Information

Chemical Name:Citreomontanine
CAS No.:74474-66-1
Molecular Formula:C₂₃H₂₈O₃
Molecular Weight:352.474
Hs Code.:
Nikkaji Number:J52.999K
Wikidata:Q77373990
Metabolomics Workbench ID:113524
Mol file:74474-66-1.mol

Synonyms:citreomontanin;citreomontanine

Suppliers and Price of Citreomontanine

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

Total 4 raw suppliers

Chemical Property of Citreomontanine

Chemical Property:

Vapor Pressure:9.3E-12mmHg at 25°C
Boiling Point:540.7°C at 760 mmHg
Flash Point:235.6°C
PSA：39.44000
Density:1.02g/cm³
LogP:5.94120
XLogP3:6.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:352.20384475
Heavy Atom Count:26
Complexity:763

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC=C(C)C=C(C)C=C(C)C=CC=CC=CC1=C(C(=CC(=O)O1)OC)C
Isomeric SMILES:C/C=C(\C)/C=C(\C)/C=C(\C)/C=C/C=C/C=C/C1=C(C(=CC(=O)O1)OC)C

Technology Process of Citreomontanine

There total 23 articles about Citreomontanine 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: 2.0%

: 102103-72-0
6-<4-formylbuta-1(E),3(E)-dienyl>-4-methoxy-5-methyl-2H-pyran-2-one

: 138133-35-4
(E,E,E)-2,4,6-trimethylocta-2,4,6-trienyl(triphenyl)phosphonium bromide

: 74474-66-1
citreomontanin

Guidance literature:: With sodium methylate; In N,N-dimethyl-formamide; at 25 ℃; for 3h;

Reference yield:

: 102103-78-6
(E,E,E)-2,4,6-trimethylocta-2,4,6-trien-1-ol

: 74474-66-1
citreomontanin

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / methanol / 144 h / 25 °C

2: 2 percent / NaOMe / dimethylformamide / 3 h / 25 °C

With sodium methylate; In methanol; N,N-dimethyl-formamide;

Reference yield:

: 102103-72-0
6-<4-formylbuta-1(E),3(E)-dienyl>-4-methoxy-5-methyl-2H-pyran-2-one

: 74474-66-1
citreomontanin

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / NaBH₄ / methanol; CH₂Cl₂ / 1 h / 25 °C

2: PPh₃, tetrabromomethane / CH₂Cl₂ / 0.5 h / 25 °C

3: CH₂Cl₂ / 14 h / 25 °C

4: 1) BuLi / 1) hexane, THF, r.t., 10 min, 2) THF, 25 deg C, 2 h

With sodium tetrahydroborate; n-butyllithium; carbon tetrabromide; triphenylphosphine; In methanol; dichloromethane;