cis-7-Dodecen-1-ol

Base Information

Chemical Name:cis-7-Dodecen-1-ol
CAS No.:20056-92-2
Molecular Formula:C12H24O
Molecular Weight:184.322
Hs Code.:2905290000
European Community (EC) Number:243-488-2
DSSTox Substance ID:DTXSID20274160
Nikkaji Number:J3.787G
Wikidata:Q67866080
Metabolomics Workbench ID:3246
Mol file:20056-92-2.mol

Synonyms:cis-7-Dodecen-1-ol;20056-92-2;Looplure inhibitor;7Z-Dodecen-1-ol;(Z)-Dodec-7-enol;7-Dodecen-1-ol, (Z)-;(Z)-7-dodecenol;(Z)-dodec-7-en-1-ol;BRN 2039845;(7Z)-Dodecen-1-ol;EINECS 243-488-2;AI3-35154;(Z)-7-Dodecen-1-ol;7-Dodecenol, Z-;Z-7-Dodecen-1-ol;(Z)-7-Dodecenyl alcohol;(7Z)-7-Dodecen-1-ol;(7Z)-dodec-7-en-1-ol;7-Dodecen-1-ol,(7Z)-;SCHEMBL832483;7-Dodecen-1-ol, (7Z)-;DTXSID20274160;LMFA05000156;AKOS006283057;BS-48908;LS-63553;CS-0160250;E75789;Q67866080

Suppliers and Price of cis-7-Dodecen-1-ol

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

American Custom Chemicals Corporation
CIS-7-DODECEN-1-OL 98.00%
1G
$ 1443.75

AHH
cis-7-Dodecen-1-ol 98%
250g
$ 408.00

Total 29 raw suppliers

Chemical Property of cis-7-Dodecen-1-ol

Chemical Property:

Vapor Pressure:0.000919mmHg at 25°C
Melting Point:77.27°C (estimate)
Refractive Index:1.4531 (estimate)
Boiling Point:270.1°Cat760mmHg
Flash Point:98.8°C
PSA：20.23000
Density:0.846g/cm³
LogP:3.67560
Storage Temp.:−20°C
XLogP3:4.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:9
Exact Mass:184.182715385
Heavy Atom Count:13
Complexity:108

Purity/Quality:

93% ^*data from raw suppliers

CIS-7-DODECEN-1-OL 98.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CCCCC=CCCCCCCO
Isomeric SMILES:CCCC/C=C\CCCCCCO
Uses (7Z)-Dodecen-1-ol is a sex pheromone of the cabbage Looper Trichoplusia ni Hubner. Synthesized from threo-aleuritic acid involving a simplified Wittig reaction. It is an intermediate in the synthesis of (7Z)-Dodecenyl Acetate, which is synthezied via nucleophilic substitution reaction between the Grignard reagent of the protected bromohydrin with (Z)-2-hepten-1-yl acetate in the presence of CuI catalyst.

Technology Process of cis-7-Dodecen-1-ol

There total 49 articles about cis-7-Dodecen-1-ol 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%