Thiophene, 2-(5-bromopentyl)-3-(3-phenylpropyl)-

Base Information

Chemical Name:Thiophene, 2-(5-bromopentyl)-3-(3-phenylpropyl)-
CAS No.:142423-03-8
Molecular Formula:C18H23BrS
Molecular Weight:351.351
Hs Code.:

Synonyms:

Suppliers and Price of Thiophene, 2-(5-bromopentyl)-3-(3-phenylpropyl)-

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 Thiophene, 2-(5-bromopentyl)-3-(3-phenylpropyl)-

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Thiophene, 2-(5-bromopentyl)-3-(3-phenylpropyl)-

There total 5 articles about Thiophene, 2-(5-bromopentyl)-3-(3-phenylpropyl)- 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: 89.0%

: 142423-02-7
5-<3-(3-phenylpropyl)-2-thienyl>-1-pentanol

: 142423-03-8
1-bromo-5-<3-(3-phenylpropyl)-2-thienyl>pentane

Guidance literature:: With allyl bromide; 1,1'-carbonyldiimidazole; In acetonitrile; for 2h; Heating;
DOI:10.1021/jm00095a011

Reference yield:

: 71778-01-3
1-phenyl-3-(thiophen-3-yl)propan-1-one

: 142423-03-8
1-bromo-5-<3-(3-phenylpropyl)-2-thienyl>pentane

Guidance literature:: Multi-step reaction with 5 steps

1: 76 percent / H₂NNH₂*H₂O, KOH / various solvent(s) / 4 h / 210 °C

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

3: H₂NNH₂*H₂O, KOH / various solvent(s) / 4 h / 210 °C

4: 76 percent / LiAlH₄ / diethyl ether / 2 h / Ambient temperature

5: 89 percent / 1,1'-carbonyldiimidazole, allyl bromide / acetonitrile / 2 h / Heating

With potassium hydroxide; lithium aluminium tetrahydride; tin(IV) chloride; hydrazine hydrate; allyl bromide; 1,1'-carbonyldiimidazole; In diethyl ether; 1,2-dichloro-ethane; acetonitrile;
DOI:10.1021/jm00095a011

Reference yield:

: 120245-35-4
3-(3-phenylpropyl)thiophene

: 142423-03-8
1-bromo-5-<3-(3-phenylpropyl)-2-thienyl>pentane

Guidance literature:: Multi-step reaction with 4 steps

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

2: H₂NNH₂*H₂O, KOH / various solvent(s) / 4 h / 210 °C

3: 76 percent / LiAlH₄ / diethyl ether / 2 h / Ambient temperature

4: 89 percent / 1,1'-carbonyldiimidazole, allyl bromide / acetonitrile / 2 h / Heating

With potassium hydroxide; lithium aluminium tetrahydride; tin(IV) chloride; hydrazine hydrate; allyl bromide; 1,1'-carbonyldiimidazole; In diethyl ether; 1,2-dichloro-ethane; acetonitrile;
DOI:10.1021/jm00095a011