Prolycopene

Base Information

Chemical Name:Prolycopene
CAS No.:2361-24-2
Molecular Formula:C40H56
Molecular Weight:536.885
Hs Code.:
DSSTox Substance ID:DTXSID001318123
Nikkaji Number:J276.706F
Wikidata:Q27131930
Metabolomics Workbench ID:47051

Synonyms:All trans Lycopene;all-trans-lycopene;LYC O MATO;LYC-O-MATO;LYCOMATO;lycopene;lycopene, (13-cis)-isomer;Lycopene, (7-cis,7'-cis,9-cis,9'-cis)-isomer -;lycopene, (cis)-isomer;Pro Lycopene;Pro-Lycopene;prolycopene

Suppliers and Price of Prolycopene

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 0 raw suppliers

Chemical Property of Prolycopene

Chemical Property:

XLogP3:15.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:16
Exact Mass:536.438201786
Heavy Atom Count:40
Complexity:1050

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CCCC(=CC=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C)C)C
Isomeric SMILES:CC(=CCC/C(=C/C=C\C(=C/C=C/C(=C/C=C/C=C(/C=C/C=C(\C=C/C=C(/CCC=C(C)C)\C)/C)\C)/C)\C)/C)C

Technology Process of Prolycopene

There total 8 articles about Prolycopene 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: 70.0%

: 5056-17-7
(2E,4E,6E)-2,7-dimethyl-2,4,6-octatrienedial

: 145571-84-2
Triphenyl<(2E,4E,6Z)-3,7,11-trimethyldodeca-2,4,6,10-tetraenyl>phosphonium Bromide

: 502-65-8,2361-24-2,4418-71-7,13018-46-7,16840-24-7,57793-70-1,58001-82-4,59092-07-8,64727-64-6,71771-86-3,71869-49-3,101468-86-4,101468-87-5,124150-08-9,145633-21-2,145633-22-3,145678-42-8,145678-43-9,145678-44-0,145678-45-1,145678-46-2
(5Z,5'Z)-Lycopene

Guidance literature:: With sodium methylate; In dichloromethane; at 0 ℃; for 0.5h;
DOI:10.1002/hlca.19920750611

Reference yield:

: 58689-15-9,3548-78-5
pseudoionone

: 502-65-8,2361-24-2,4418-71-7,13018-46-7,16840-24-7,57793-70-1,58001-82-4,59092-07-8,64727-64-6,71771-86-3,71869-49-3,101468-86-4,101468-87-5,124150-08-9,145633-21-2,145633-22-3,145678-42-8,145678-43-9,145678-44-0,145678-45-1,145678-46-2
(5Z,5'Z)-Lycopene

Guidance literature:: Multi-step reaction with 4 steps

1: 1) Li, liq. NH₃ / 2) THF, 10 deg C, 5 min

2: H₂, 2,2'-(ethylenedithio)bis(ethanol), Et₃N / Lindlar catalyst / CH₂Cl₂ / 750.06 Torr / Ambient temperature

3: 8.5 percent / methanol / Ambient temperature

4: 70 percent / 3M methanol. NaOMe / CH₂Cl₂ / 0.5 h / 0 °C

With 2,2'-ethane-1,2-diylbissulfanyl-bis-ethanol; ammonia; hydrogen; sodium methylate; lithium; triethylamine; Lindlar's catalyst; In methanol; dichloromethane;
DOI:10.1002/hlca.19920750611

Reference yield:

: 20082-23-9,145571-82-0,145571-83-1
(4E,6E/Z)-3,7,11-Trimethyldodeca-4,6,10-trien-1-yn-3-ol

: 502-65-8,2361-24-2,4418-71-7,13018-46-7,16840-24-7,57793-70-1,58001-82-4,59092-07-8,64727-64-6,71771-86-3,71869-49-3,101468-86-4,101468-87-5,124150-08-9,145633-21-2,145633-22-3,145678-42-8,145678-43-9,145678-44-0,145678-45-1,145678-46-2
(5Z,5'Z)-Lycopene

Guidance literature:: Multi-step reaction with 3 steps

1: H₂, 2,2'-(ethylenedithio)bis(ethanol), Et₃N / Lindlar catalyst / CH₂Cl₂ / 750.06 Torr / Ambient temperature

2: 8.5 percent / methanol / Ambient temperature

3: 70 percent / 3M methanol. NaOMe / CH₂Cl₂ / 0.5 h / 0 °C

With 2,2'-ethane-1,2-diylbissulfanyl-bis-ethanol; hydrogen; sodium methylate; triethylamine; Lindlar's catalyst; In methanol; dichloromethane;
DOI:10.1002/hlca.19920750611