Laurifine

Base Information

Chemical Name:Laurifine
CAS No.:56261-28-0
Molecular Formula:C19H23NO3
Molecular Weight:313.3908
Hs Code.:
DSSTox Substance ID:DTXSID10331791
Nikkaji Number:J2.770.097G
Wikidata:Q27107191
Metabolomics Workbench ID:69241

Synonyms:Laurifine;56261-28-0;C09565;4,5,16-trimethoxy-10-azatricyclo[11.4.0.02,7]heptadeca-1(13),2,4,6,14,16-hexaene;AC1L9CKQ;CHEBI:6391;DTXSID10331791;Q27107191

Suppliers and Price of Laurifine

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 0 raw suppliers

Chemical Property of Laurifine

Chemical Property:

Vapor Pressure:9.55E-10mmHg at 25°C
Boiling Point:489.9°Cat760mmHg
Flash Point:203.1°C
PSA：39.72000
Density:1.09g/cm³
LogP:3.39640
XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:313.16779360
Heavy Atom Count:23
Complexity:365

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC2=C(CCNCCC3=CC(=C(C=C32)OC)OC)C=C1

Technology Process of Laurifine

There total 10 articles about Laurifine 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:

: 92827-58-2
8,9-dimethoxy-2,3,5,6-tetrahydro-1H-pyrrolo<2,1-a>isoquinolinium chloride

: 56261-28-0
Laurifin

Guidance literature:: Multi-step reaction with 7 steps

1: 84 percent / 40percent aq. NaOH / 0 °C

2: 34 percent / ethanol / 6 h / Heating

3: 74 percent / K₂CO₃ / benzene / 1.) reflux, 8 h, 2.) RT, 12 h

4: 95 percent / CuBr₂ / 1.5 h / Heating

5: 89 percent / LiAlH₄ / tetrahydrofuran / 1.5 h / Heating

6: 59 percent / CH₂Cl₂ / 24 h / Ambient temperature

7: LiAlH₄ / tetrahydrofuran / 2 h / Heating

With sodium hydroxide; lithium aluminium tetrahydride; potassium carbonate; copper(ll) bromide; In tetrahydrofuran; ethanol; dichloromethane; benzene;

Reference yield:

: 120-20-7
2-(3,4-dimethoxyphenyl)-ethylamine

: 56261-28-0
Laurifin

Guidance literature:: Multi-step reaction with 8 steps

1: 83 percent / POCl₃ / toluene / 3 h / Heating

2: 84 percent / 40percent aq. NaOH / 0 °C

3: 34 percent / ethanol / 6 h / Heating

4: 74 percent / K₂CO₃ / benzene / 1.) reflux, 8 h, 2.) RT, 12 h

5: 95 percent / CuBr₂ / 1.5 h / Heating

6: 89 percent / LiAlH₄ / tetrahydrofuran / 1.5 h / Heating

7: 59 percent / CH₂Cl₂ / 24 h / Ambient temperature

8: LiAlH₄ / tetrahydrofuran / 2 h / Heating

With sodium hydroxide; lithium aluminium tetrahydride; potassium carbonate; copper(ll) bromide; trichlorophosphate; In tetrahydrofuran; ethanol; dichloromethane; toluene; benzene;