Pomarose

Base Information

Chemical Name:Pomarose
CAS No.:357650-26-1
Molecular Formula:C₁₁H₁₈O
Molecular Weight:166.26
Hs Code.:
European Community (EC) Number:879-169-5
UNII:EPU9H8QVS8
DSSTox Substance ID:DTXSID00889170
Nikkaji Number:J1.589.122J
Wikipedia:Pomarose
Wikidata:Q2103259
Mol file:357650-26-1.mol

Synonyms:Pomarose;EPU9H8QVS8;357650-26-1;2,5-Octadien-4-one, 5,6,7-trimethyl-, (2E,5Z)-;UNII-EPU9H8QVS8;(2E,5Z)-5,6,7-Trimethyl-2,5-octadien-4-one;(2E,5Z)-5,6,7-trimethylocta-2,5-dien-4-one;SCHEMBL6761885;DTXSID00889170;(2E,5Z)-5,6,7-Trimethyl-2,5-octadiene-4-one;Q2103259

Suppliers and Price of Pomarose

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 15 raw suppliers

Chemical Property of Pomarose

Chemical Property:

Vapor Pressure:0.048mmHg at 25°C
Boiling Point:236.15°C at 760 mmHg
Flash Point:89.352°C
Density:0.855g/cm³
XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:166.135765193
Heavy Atom Count:12
Complexity:219

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC=CC(=O)C(=C(C)C(C)C)C
Isomeric SMILES:C/C=C/C(=O)/C(=C(/C)\C(C)C)/C

Technology Process of Pomarose

There total 4 articles about Pomarose 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:

: 563-80-4
3-methyl-butan-2-one

: 357650-26-1
(2E,5Z)-5,6,7-trimethylocta-2,5-dien-4-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: BF₃*Et₂O / diethyl ether / 0.17 h / -15 °C

1.2: 59 percent / diethyl ether / 1 h / 0 °C

2.1: LDA / tetrahydrofuran; hexane / 1 h / Heating

With boron trifluoride diethyl etherate; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; hexane; 2.1: Grignard reaction;
DOI:10.1002/1099-0690(200106)2001:12<2363::AID-EJOC2363>3.0.CO;2-E

Reference yield:

: 563-80-4
3-methyl-butan-2-one

: 357650-26-1
(2E,5E)-5,6,7-trimethylocta-2,5-dien-4-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: BF₃*Et₂O / diethyl ether / 0.17 h / -15 °C

1.2: 59 percent / diethyl ether / 1 h / 0 °C

2.1: LDA / tetrahydrofuran; hexane / 1 h / Heating

With boron trifluoride diethyl etherate; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; hexane; 2.1: Grignard reaction;
DOI:10.1002/1099-0690(200106)2001:12<2363::AID-EJOC2363>3.0.CO;2-E

Reference yield:

: 13154-14-8,13154-15-9,14092-04-7,1730-25-2
1-propenylmagnesium bromide

: 6570-81-6
(2E/Z)-ethyl 2,3,4-trimethylpent-2-enoate

: 357650-26-1
(2E,5Z)-5,6,7-trimethylocta-2,5-dien-4-one

: 357650-26-1
(2E,5E)-5,6,7-trimethylocta-2,5-dien-4-one

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; hexane; for 1h; Heating;
DOI:10.1002/1099-0690(200106)2001:12<2363::AID-EJOC2363>3.0.CO;2-E