Solanesyl Acetone

Base Information

Chemical Name:Solanesyl Acetone
CAS No.:65717-26-2
Molecular Formula:C48H78O
Molecular Weight:671.13200
Hs Code.:
European Community (EC) Number:924-563-5
DSSTox Substance ID:DTXSID301316233
Nikkaji Number:J416.594B,J24.209H

Synonyms:65717-26-2;Solanesyl Acetone;(5E,9E,13E,17E,21E,25E,29E,33E)-6,10,14,18,22,26,30,34,38-nonamethylnonatriaconta-5,9,13,17,21,25,29,33,37-nonaen-2-one;SCHEMBL7944866;DTXSID301316233

Suppliers and Price of Solanesyl Acetone

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
SolanesylAcetone
250mg
$ 825.00

TRC
SolanesylAcetone
5mg
$ 85.00

Total 0 raw suppliers

Chemical Property of Solanesyl Acetone

Chemical Property:

Vapor Pressure:2.72E-20mmHg at 25°C
PSA：17.07000
LogP:16.13380
XLogP3:16.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:27
Exact Mass:670.60526711
Heavy Atom Count:49
Complexity:1210

Purity/Quality:: SolanesylAcetone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=O)C)C)C)C)C)C)C)C)C)C
Isomeric SMILES:CC(=CCC/C(=C/CC/C(=C/CC/C(=C/CC/C(=C/CC/C(=C/CC/C(=C/CC/C(=C/CC/C(=C/CCC(=O)C)/C)/C)/C)/C)/C)/C)/C)/C)C
Uses Solanesyl Acetone is an intermediate in the synthesis of Isodecaprenol, a side chain of coenzyme Q10.

Technology Process of Solanesyl Acetone

There total 4 articles about Solanesyl Acetone 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: 58.0%

: 80868-10-6
(5E,9E,13E,17E,21E,25E,29E,33E)-6,10,14,18,22,26,30,34,38-Nonamethyl-3-(toluene-4-sulfonyl)-nonatriaconta-5,9,13,17,21,25,29,33,37-nonaen-2-one

: 65717-26-2,75538-85-1
Solanesylacetone

Guidance literature:: With disodium hydrogenphosphate; sodium amalgam; In methanol; diethyl ether; at 0 ℃; for 8h;
DOI:10.1055/s-1981-29599

Reference yield:

: 909247-30-9
(4E,8E,12E,16E,20E,24E,28E,32E)-2-Acetyl-5,9,13,17,21,25,29,33,37-nonamethyl-octatriaconta-4,8,12,16,20,24,28,32,36-nonaenoic acid ethyl ester

: 65717-26-2,75538-85-1
Solanesylacetone

Guidance literature:: With sodium hydroxide; In ethanol; Yield given; 1.) r.t., 2 h, 2.) 60 deg C, 3 h;
DOI:10.1002/recl.19941130305

Reference yield:

: 13190-97-1,540-03-4
solanesol

: 65717-26-2,75538-85-1
Solanesylacetone

Guidance literature:: Multi-step reaction with 3 steps

1: PBr₃ / pyridine / diethyl ether; petroleum ether / 2 h / 0 °C

2: Na / ethanol / 1,) 0 deg C, 3 h, 2.) 60 deg C, 4 h, 3.) r.t., overnight

3: 10percent aq. NaOH / ethanol / 1.) r.t., 2 h, 2.) 60 deg C, 3 h

With sodium hydroxide; sodium; phosphorus tribromide; pyridine; In diethyl ether; ethanol; Petroleum ether;
DOI:10.1002/recl.19941130305