Ar-Curcumene

Base Information

Chemical Name:Ar-Curcumene
CAS No.:4176-06-1
Molecular Formula:C₁₅H₂₂
Molecular Weight:202.34
Hs Code.:
DSSTox Substance ID:DTXSID00905046
Nikkaji Number:J37.671J
Wikidata:Q81983415
Metabolomics Workbench ID:75307
Mol file:4176-06-1.mol

Synonyms:(R)-isomer of alpha-curcumene;(S)-isomer of alpha-curcumene;1-(1,5-dimethyl-4-hexenyl)-4-methylbenzene;2-methyl-6-p-tolyl-2-heptene;alpha-curcumene;ar-curcumene

Suppliers and Price of Ar-Curcumene

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
(S)-ar-Curcumene
100mg
$ 3150.00

TRC
(S)-ar-Curcumene
10mg
$ 485.00

Total 9 raw suppliers

Chemical Property of Ar-Curcumene

Chemical Property:

Vapor Pressure:0.00814mmHg at 25°C
Boiling Point:276.3°C at 760 mmHg
Flash Point:117.2°C
PSA：0.00000
Density:0.873g/cm³
LogP:4.84490
XLogP3:5.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:4
Exact Mass:202.172150702
Heavy Atom Count:15
Complexity:190

Purity/Quality:

Analysis control,98.0% ^*data from raw suppliers

(S)-ar-Curcumene ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)C(C)CCC=C(C)C
Isomeric SMILES:CC1=CC=C(C=C1)[C@@H](C)CCC=C(C)C
Uses (S)-ar-Curcumene is used in the study and the characterization of the antioxidant and antimicrobial compounds of cinnamon and ginger essential oils, also in the phytochemical and biological studies of the flower and fruits of Pongamia pinnata.

Technology Process of Ar-Curcumene

There total 136 articles about Ar-Curcumene 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: 97.0%

: C₁₅H₁₉F₃O₃S

: 75-16-1
methylmagnesium bromide

: 3649-81-8,4176-17-4,644-30-4,4176-06-1
(S)-curcumene

Guidance literature:: With iron(III)-acetylacetonate; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; diethyl ether; at 0 ℃; for 0.25h;
DOI:10.1021/ja1034842

Reference yield: 89.0%

: 1580457-76-6
(S)-5-methyl-2-(6-methylhept-5-en-2-yl)benzoic acid

: 3649-81-8,4176-17-4,644-30-4,4176-06-1
(S)-curcumene

Guidance literature:: With quinoline; copper; at 20 ℃; for 3h; Inert atmosphere;
DOI:10.1039/c4ob00018h

Reference yield: 79.0%

: 122091-57-0
(-)-(R)-4-(p-tolyl)pentanal

: 24470-78-8
isopropyltriphenylphosphonium iodide

: 4176-17-4,644-30-4,3649-81-8,4176-06-1
(R)-(-)-α-curcumene

Guidance literature:: isopropyltriphenylphosphonium iodide; With n-butyllithium; In tetrahydrofuran; hexane; at -15 ℃; for 0.583333h; Inert atmosphere;

(-)-(R)-4-(p-tolyl)pentanal; In tetrahydrofuran; hexane; at 0 - 20 ℃; for 0.5h; Inert atmosphere;
DOI:10.1016/j.tetasy.2015.11.009