1,1-Diethoxycyclopentane

Base Information

Chemical Name:1,1-Diethoxycyclopentane
CAS No.:23786-93-8
Molecular Formula:C9H18 O2
Molecular Weight:158.241
Hs Code.:2911000000
European Community (EC) Number:245-888-2
UNII:BU0U0V23NM
DSSTox Substance ID:DTXSID40178474
Nikkaji Number:J242.682J
Wikidata:Q83048881
Mol file:23786-93-8.mol

Synonyms:1,1-Diethoxycyclopentane;23786-93-8;Cyclopentane, 1,1-diethoxy-;EINECS 245-888-2;BU0U0V23NM;starbld0001243;Sodium zinc metasilicate;1,1-diethoxy-cyclopentane;UNII-BU0U0V23NM;SCHEMBL732380;DTXSID40178474;AKOS028110934

Suppliers and Price of 1,1-Diethoxycyclopentane

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
1,1-Diethoxycyclopentane
2.5g
$ 230.00

TRC
1,1-Diethoxycyclopentane
1g
$ 115.00

Total 4 raw suppliers

Chemical Property of 1,1-Diethoxycyclopentane

Chemical Property:

Vapor Pressure:1.08mmHg at 25°C
Boiling Point:183°Cat760mmHg
Flash Point:49.6°C
PSA：18.46000
Density:0.92g/cm³
LogP:2.32970
XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:158.130679813
Heavy Atom Count:11
Complexity:98.1

Purity/Quality:

99% ^*data from raw suppliers

1,1-Diethoxycyclopentane ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC1(CCCC1)OCC
Uses 1,1-Diethoxycyclopentane is a reagent that is used in the synthesis of Quinbolone (Q670150), which is a cyclopentenyl ether derivative of Boldenone (B675100) and also its active metabolite. Quinbolone shows weak androgenic activity.

Technology Process of 1,1-Diethoxycyclopentane

There total 6 articles about 1,1-Diethoxycyclopentane 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%

: 122-51-0
orthoformic acid triethyl ester

: 120-92-3
cyclopentanone

: 23786-93-8
1,1-diethoxy-cyclopentane

Guidance literature:: With Sulfate; titanium(IV) oxide; In ethanol; for 0.583333h; Heating;
DOI:10.1081/SCC-120021036

Reference yield: 85.0%

: 64-17-5
ethanol

: 120-92-3
cyclopentanone

: 23786-93-8
1,1-diethoxy-cyclopentane

Guidance literature:: cadmium(II) iodide; for 0.025h; microwave irradiation;
DOI:10.1246/cl.1999.1283

Reference yield:

: 142-29-0
cyclopentene

: 105-57-7,30846-29-8
diethyl acetal

: 23786-93-8
1,1-diethoxy-cyclopentane

: 17065-24-6
1-ethoxycyclopentene

: 120-92-3
cyclopentanone

Guidance literature:: With oxygen; p-benzoquinone; palladium dichloride; In ethanol; at 30 ℃; for 8h; under 860 Torr; Product distribution;
DOI:10.1246/cl.1985.1835