(+)-Aromadendrene

Base Information

Chemical Name:(+)-Aromadendrene
CAS No.:72747-25-2
Molecular Formula:C₁₅H₂₄
Molecular Weight:204.356
Hs Code.:
European Community (EC) Number:207-694-6
DSSTox Substance ID:DTXSID60862020,DTXSID80881253
Nikkaji Number:J12.596B
Wikidata:Q76416625
Metabolomics Workbench ID:127658
ChEMBL ID:CHEMBL2269083

Synonyms:aromadendrene

Suppliers and Price of (+)-Aromadendrene

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 3 raw suppliers

Chemical Property of (+)-Aromadendrene

Chemical Property:

Boiling Point:258.1±7.0 °C(Predicted)
Density:0.93±0.1 g/cm3(Predicted)
XLogP3:4.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:0
Exact Mass:204.187800766
Heavy Atom Count:15
Complexity:299

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1CCC2C1C3C(C3(C)C)CCC2=C
Isomeric SMILES:C[C@@H]1CC[C@@H]2[C@@H]1[C@H]3[C@H](C3(C)C)CCC2=C

Technology Process of (+)-Aromadendrene

There total 4 articles about (+)-Aromadendrene 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:

: 27200-84-6
methyl triphenylphosphonium bromide

: 6790-66-5,14682-45-2,14917-87-4,95977-69-8,97275-30-4,97950-12-4,99147-41-8
(-)-apoaromadendrone

: 489-39-4,552-01-2,14682-34-9,14682-39-4,14682-40-7,14682-42-9,25246-27-9,55721-09-0,72747-25-2,74036-37-6,97950-10-2,109119-91-7,125133-80-4,146389-60-8
(+)-aromadendrene

Guidance literature:: With dimsylsodium; Yield given. Multistep reaction; 1) dimethyl sulfoxide, r.t., 30 min., 2) ether, r.t., 2 h;
DOI:10.1016/S0040-4020(01)87904-7

Reference yield:

: 6790-66-5,14682-45-2,14917-87-4,95977-69-8,97275-30-4,97950-12-4,99147-41-8
(-)-apoaromadendrone

: 489-39-4,552-01-2,14682-34-9,14682-39-4,14682-40-7,14682-42-9,25246-27-9,55721-09-0,72747-25-2,74036-37-6,97950-10-2,109119-91-7,125133-80-4,146389-60-8
(-)-alloaromadendrene

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / Et₃N / dimethylformamide / 48 h / Heating

2: 99 percent / Et₃N / methanol / 4 h / -20 °C

With triethylamine; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(01)88765-2

Reference yield:

: 141564-33-2
Trimethyl-((1aR,7R,7aS,7bR)-1,1,7-trimethyl-1a,2,3,5,6,7,7a,7b-octahydro-1H-cyclopropa[e]azulen-4-yloxy)-silane

: 489-39-4,552-01-2,14682-34-9,14682-39-4,14682-40-7,14682-42-9,25246-27-9,55721-09-0,72747-25-2,74036-37-6,97950-10-2,109119-91-7,125133-80-4,146389-60-8
(-)-alloaromadendrene

Guidance literature:: Multi-step reaction with 2 steps

1: 99 percent / Et₃N / methanol / 4 h / -20 °C

With triethylamine; In methanol;
DOI:10.1016/S0040-4020(01)88765-2