2-Oxepanone, 7-methyl-, (7R)-

Base Information

Chemical Name:2-Oxepanone, 7-methyl-, (7R)-
CAS No.:69765-34-0
Molecular Formula:C7H12O2
Molecular Weight:128.171
Hs Code.:
DSSTox Substance ID:DTXSID30458237
Nikkaji Number:J1.424.792K
Wikidata:Q82281433

Synonyms:2-Oxepanone, 7-methyl-, (7R)-;69765-34-0;(R)-7-Methyloxepane-2-one;SCHEMBL15248047;DTXSID30458237

Suppliers and Price of 2-Oxepanone, 7-methyl-, (7R)-

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 2-Oxepanone, 7-methyl-, (7R)-

Chemical Property:

XLogP3:1.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:128.083729621
Heavy Atom Count:9
Complexity:110

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CCCCC(=O)O1
Isomeric SMILES:C[C@@H]1CCCCC(=O)O1

Technology Process of 2-Oxepanone, 7-methyl-, (7R)-

There total 4 articles about 2-Oxepanone, 7-methyl-, (7R)- 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: 40.0%

: 2549-59-9
7-methyl-2-oxepanone

: 3319-15-1
rac-1-(4-methoxyphenyl)-ethanol

: 1517-70-0,1572-97-0,3319-15-1,43230-31-5
(S)-1-(4-Methoxyphenyl)ethanol

: 1517-70-0
(R)-1-(4-Methoxyphenyl)ethanol

: (R)-1-(4-methoxyphenyl)ethyl-(S)-6-hydroxyheptanoate

: 69765-35-1
(6S)-6-methyl-ε-caprolactone

: 69765-34-0
(6R)-6-methyl-ε-caprolactone

Guidance literature:: With lipase B from Candida antarctica; In toluene; at 37 ℃; for 60h; enantioselective reaction; Enzymatic reaction;
DOI:10.1002/cctc.201402672

Reference yield:

: 2549-59-9
7-methyl-2-oxepanone

: 877-65-6
p-tert-butylbenzyl alcohol

: C₁₈H₂₈O₃

: C₁₈H₂₈O₃

: 69765-35-1
(6S)-6-methyl-ε-caprolactone

: 69765-34-0
(6R)-6-methyl-ε-caprolactone

Guidance literature:: With Novozym 435; In toluene; at 20 ℃; for 3h; Further byproducts. Title compound not separated from byproducts.;
DOI:10.1016/j.tetasy.2007.03.016

Reference yield:

: 583-60-8
2-Methylcyclohexanone

: 69765-35-1
(6S)-6-methyl-ε-caprolactone

: 69765-34-0
(6R)-6-methyl-ε-caprolactone

: 126372-25-6
(S)-6-Hydroxy-heptanoic acid

: 21961-03-5,50516-06-8,126372-25-6
(R)-6-hydroxyheptanoic acid

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; for 5h; Yield given. Yields of byproduct given;
DOI:10.1055/s-1989-27351