2,5-Cyclohexadiene-1,4-dione, 2,3-dimethoxy-5-methyl-6-(3,7,11-trimethyl-2,6,10-dodecatrienyl)-, (E,E)-

Base Information

Chemical Name:2,5-Cyclohexadiene-1,4-dione, 2,3-dimethoxy-5-methyl-6-(3,7,11-trimethyl-2,6,10-dodecatrienyl)-, (E,E)-
CAS No.:1173-76-8
Molecular Formula:C24H34 O4
Molecular Weight:386.532
Hs Code.:
Nikkaji Number:J2.138.902A,J93.223J
ChEMBL ID:CHEMBL4166910

Synonyms:coenzyme Q3;CoQ3;ubiquinone Q3

Suppliers and Price of 2,5-Cyclohexadiene-1,4-dione, 2,3-dimethoxy-5-methyl-6-(3,7,11-trimethyl-2,6,10-dodecatrienyl)-, (E,E)-

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 1 raw suppliers

Chemical Property of 2,5-Cyclohexadiene-1,4-dione, 2,3-dimethoxy-5-methyl-6-(3,7,11-trimethyl-2,6,10-dodecatrienyl)-, (E,E)-

Chemical Property:

PSA：52.60000
LogP:5.76840
XLogP3:6.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:10
Exact Mass:386.24570956
Heavy Atom Count:28
Complexity:754

Purity/Quality:: 95%+ or 98%+ ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 2,5-Cyclohexadiene-1,4-dione, 2,3-dimethoxy-5-methyl-6-(3,7,11-trimethyl-2,6,10-dodecatrienyl)-, (E,E)-

There total 35 articles about 2,5-Cyclohexadiene-1,4-dione, 2,3-dimethoxy-5-methyl-6-(3,7,11-trimethyl-2,6,10-dodecatrienyl)-, (E,E)- 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: 93.0%

: 5-farnesyl-2,3,4-trimethoxy-6-methylphenol

: 1173-76-8
ubiquinone Q₃

Guidance literature:: With iron(III) chloride; In ethanol; water; at 20 ℃; for 2h;
DOI:10.1080/00397910701771066

Reference yield: 86.0%

: 8a-[(all-E)-3,7,11-trimethyl-2,6,10-dodecatrienyl]-1,4,4a,8a-tetrahydro-6,7-dimethoxy-4a-methyl-1,4-methano[4a,8a-13C₂]naphthalene-5,8-dione

: 1173-76-8
[5,6-13C₂] 2,5-cyclohexadiene-1,4-dione, 2,3-dimethoxy-5-methyl-6-(3,7,11-trimethyl-2,6,10-dodecatrienyl)-, (E,E)-

Guidance literature:: In toluene; for 0.333333h; Heating;
DOI:10.1002/(SICI)1099-1344(199807)41:7<657::AID-JLCR110>3.0.CO;2-E

Reference yield: 84.0%

: 22850-55-1
(E)-6,10-dimethyl-5,9-undecadien-1-yne

: 75-24-1
trimethylaluminum

: 202843-56-9
2-chloromethyl-5,6-dimethoxy-3-methyl-[1,4]benzoquinone

: 1173-76-8
ubiquinone Q₃

Guidance literature:: (E)-6,10-dimethyl-5,9-undecadien-1-yne; trimethylaluminum; With zirconocene dichloride; In hexane; 1,2-dichloro-ethane;

2-chloromethyl-5,6-dimethoxy-3-methyl-[1,4]benzoquinone; With bis(triphenylphosphine)nickel(II) chloride; n-butyllithium; In tetrahydrofuran; hexane;
DOI:10.1021/ja992164p