1-Cyclopentene-1-methanol, acetate

Base Information

Chemical Name:1-Cyclopentene-1-methanol, acetate
CAS No.:53723-45-8
Molecular Formula:C8H12O2
Molecular Weight:140.1797
Hs Code.:
DSSTox Substance ID:DTXSID80201992
Nikkaji Number:J275.672B
Wikidata:Q83075235

Synonyms:1-Cyclopentene-1-methanol, acetate;53723-45-8;DTXSID80201992;1-Cyclopentene-1-methanol acetate

Suppliers and Price of 1-Cyclopentene-1-methanol, acetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-Cyclopentene-1-methanol, acetate

Chemical Property:

Vapor Pressure:0.832mmHg at 25°C
Boiling Point:181.9°Cat760mmHg
Flash Point:80.9°C
Density:1.019g/cm³
XLogP3:1.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:140.083729621
Heavy Atom Count:10
Complexity:159

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=O)OCC1=CCCC1

Technology Process of 1-Cyclopentene-1-methanol, acetate

There total 6 articles about 1-Cyclopentene-1-methanol, acetate 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:

: 693-89-0
1-methylcyclopent-1-ene

: 64-19-7,77671-22-8
acetic acid

: 53723-45-8
(1-cyclopenten-1-yl)methyl acetate

: 53723-44-7
2-methylenecyclopenten-1-yl acetate

: 92984-84-4
2-methylcyclopent-2-en-1-yl acetate

: 124021-35-8
1-methyl-3-cyclopenten-1-yl acetate

Guidance literature:: With manganese(IV) oxide; p-benzoquinone; palladium diacetate; at 40 ℃; for 48h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1021/jo00290a031