(8)-Shogaol

Base Information

Chemical Name:(8)-Shogaol
CAS No.:36700-45-5
Molecular Formula:C19H28O3
Molecular Weight:304.4238
Hs Code.:
UNII:AV4IK2HCNT
Nikkaji Number:J506.158J
Wikidata:Q27274135
Metabolomics Workbench ID:44894
ChEMBL ID:CHEMBL25893
Mol file:36700-45-5.mol

Synonyms:(8)-shogaol;8-shogaol

Suppliers and Price of (8)-Shogaol

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
8-?Shogaol
25mg
$ 775.00

JR MediChem
8-shogaol(NewProduct) 98%
20mg
$ 468.00

Crysdot
8-Shogaol 97%
5mg
$ 410.00

ChemScene
[8]-Shogaol 99.74%
10mg
$ 457.00

Biorbyt Ltd
8-Shogaol 98%
10 mg
$ 445.40

AvaChem
8-Shogaol
1mg
$ 290.00

AvaChem
8-Shogaol
5mg
$ 690.00

AvaChem
8-Shogaol
20mg
$ 1690.00

Arctom
8-Shogaol
100mg
$ 1301.00

Arctom
8-Shogaol
5mg
$ 318.00

Total 32 raw suppliers

Chemical Property of (8)-Shogaol

Chemical Property:

Vapor Pressure:8.45E-09mmHg at 25°C
Boiling Point:452.3°Cat760mmHg
PKA:10.01±0.20(Predicted)
Flash Point:154.6°C
PSA：46.53000
Density:1.013g/cm³
LogP:4.81920
XLogP3:4.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:11
Exact Mass:304.20384475
Heavy Atom Count:22
Complexity:325

Purity/Quality:

≥98% ^*data from raw suppliers

8-?Shogaol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCC=CC(=O)CCC1=CC(=C(C=C1)O)OC
Isomeric SMILES:CCCCCCC/C=C/C(=O)CCC1=CC(=C(C=C1)O)OC
Uses 8-?Shogaol is a component of ginger (Zingiber officinale) and maintains anti-inflammatory activity as a cyclooxygenase-2 inhibitor.

Technology Process of (8)-Shogaol

There total 10 articles about (8)-Shogaol 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: 95.0%

: 77398-92-6
5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)dodecan-3-one

: 36700-45-5,104186-07-4
[8]-shogaol

Guidance literature:: With hydrogenchloride; In tetrahydrofuran; for 4h; Heating;
DOI:10.1080/00397919908086182

Reference yield: 57.0%

: 124-13-0
Octanal

: 122-48-5
4-(4-hydroxy-3-methoxyphenyl)-2-butanone

: 36700-45-5,104186-07-4
[8]-shogaol

Guidance literature:: With DIMCARB; at 20 ℃; for 72h;
DOI:10.1039/c9ob02662b

Reference yield: 47.0%

: 77398-92-6
5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)dodecan-3-one

: 36700-45-5,104186-07-4
[8]-shogaol

: 23513-08-8,77398-92-6,107257-17-0,135272-33-2
[8]-gingerol

Guidance literature:: With potassium fluoride; C₅₀H₃₄F₁₂O₆; In toluene; at 25 ℃; for 192h; enantioselective reaction; Inert atmosphere; Resolution of racemate;
DOI:10.1021/acs.orglett.8b00547