7-[5-(3-Phenylpropyl)thiophen-3-yl]heptanoic acid

Base Information

Chemical Name:7-[5-(3-Phenylpropyl)thiophen-3-yl]heptanoic acid
CAS No.:142422-48-8
Molecular Formula:C20H26O2S
Molecular Weight:330.491
Hs Code.:
ChEMBL ID:CHEMBL106054
DSSTox Substance ID:DTXSID50576568
Nikkaji Number:J491.907F
Wikidata:Q82466340

Synonyms:142422-48-8;7-[5-(3-Phenylpropyl)thiophen-3-yl]heptanoic acid;CHEMBL106054;SCHEMBL17833684;DTXSID50576568

Suppliers and Price of 7-[5-(3-Phenylpropyl)thiophen-3-yl]heptanoic acid

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 1 raw suppliers

Chemical Property of 7-[5-(3-Phenylpropyl)thiophen-3-yl]heptanoic acid

Chemical Property:

XLogP3:6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:11
Exact Mass:330.16535124
Heavy Atom Count:23
Complexity:326

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CCCC2=CC(=CS2)CCCCCCC(=O)O

Technology Process of 7-[5-(3-Phenylpropyl)thiophen-3-yl]heptanoic acid

There total 4 articles about 7-[5-(3-Phenylpropyl)thiophen-3-yl]heptanoic acid 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: 92.0%

: 142422-85-3
ethyl 7-<5-(3-phenylpropionyl)-3-thienyl>heptanoate

: 142422-48-8
7-<5-(3-phenylpropyl)-3-thienyl>heptanoic acid

Guidance literature:: With potassium hydroxide; hydrazine hydrate; In various solvent(s); at 210 ℃; for 4h;
DOI:10.1021/jm00095a011

Reference yield:

: 142422-84-2
7-(3-thienyl)heptanoate d'ethyle

: 142422-48-8
7-<5-(3-phenylpropyl)-3-thienyl>heptanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 92.8 percent / N-bromosuccinimide / ethyl acetate; CHCl₃ / 0.03 h

2: 61 percent / SnCl₄ / 1,2-dichloro-ethane / 1 h / Ambient temperature

3: 50 percent / Zn, acetic acid / H₂O / 24 h / Ambient temperature

4: 92 percent / H₂NNH₂*H₂₀, KOH / various solvent(s) / 4 h / 210 °C

With potassium hydroxide; N-Bromosuccinimide; tin(IV) chloride; hydrazine hydrate; acetic acid; zinc; In chloroform; water; ethyl acetate; 1,2-dichloro-ethane;
DOI:10.1021/jm00095a011

Reference yield:

: 142422-94-4
ethyl 7-(2-bromo-3-thienyl)heptanoate

: 142422-48-8
7-<5-(3-phenylpropyl)-3-thienyl>heptanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 61 percent / SnCl₄ / 1,2-dichloro-ethane / 1 h / Ambient temperature

2: 50 percent / Zn, acetic acid / H₂O / 24 h / Ambient temperature

3: 92 percent / H₂NNH₂*H₂₀, KOH / various solvent(s) / 4 h / 210 °C

With potassium hydroxide; tin(IV) chloride; hydrazine hydrate; acetic acid; zinc; In water; 1,2-dichloro-ethane;
DOI:10.1021/jm00095a011