Hexanoic acid, 6-(phenylmethoxy)-

Base Information

Chemical Name:Hexanoic acid, 6-(phenylmethoxy)-
CAS No.:130892-97-6
Molecular Formula:C13H18O3
Molecular Weight:222.284
Hs Code.:
DSSTox Substance ID:DTXSID30435684
Nikkaji Number:J687.077E
Wikidata:Q82250748

Synonyms:Hexanoic acid, 6-(phenylmethoxy)-;130892-97-6;6-benzyloxyhexanoic acid;6-(BENZYLOXY)HEXANOIC ACID;6-phenylmethoxyhexanoic Acid;6-benzyloxy-hexanoic acid;SCHEMBL830483;DTXSID30435684;IILIIPOEUNIPFG-UHFFFAOYSA-N;AKOS013620053;A903823

Suppliers and Price of Hexanoic acid, 6-(phenylmethoxy)-

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 5 raw suppliers

Chemical Property of Hexanoic acid, 6-(phenylmethoxy)-

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:8
Exact Mass:222.125594432
Heavy Atom Count:16
Complexity:186

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COCCCCCC(=O)O

Technology Process of Hexanoic acid, 6-(phenylmethoxy)-

There total 13 articles about Hexanoic acid, 6-(phenylmethoxy)- 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: 94.0%

: 101492-91-5
6-benzyloxy-1-hexanal

: 130892-97-6
6-benzyloxyhexanoic acid

Guidance literature:: With sodium chlorite; sodium dihydrogenphosphate; 2-methyl-but-2-ene; In water; tert-butyl alcohol; at 20 ℃; for 1h;
DOI:10.1016/j.tet.2013.01.048