Thiophene, 2-[(1S)-3-chloro-1-(1-naphthalenyloxy)propyl]-

Base Information

Chemical Name:Thiophene, 2-[(1S)-3-chloro-1-(1-naphthalenyloxy)propyl]-
CAS No.:164071-61-8
Molecular Formula:C17H15ClOS
Molecular Weight:302.824
Hs Code.:
Mol file:164071-61-8.mol

Synonyms:S-3-chloro-1-(2-thienyl)-1-(1-naphthalenyloxy)propane;2-[(S)-3-Chloro-1-(naphthalen-1-yloxy)-propyl]-thiophene;

Suppliers and Price of Thiophene, 2-[(1S)-3-chloro-1-(1-naphthalenyloxy)propyl]-

Supply Marketing:

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

Manufacturers and distributors:

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Chemicals and raw materials
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price

Total 3 raw suppliers

Chemical Property of Thiophene, 2-[(1S)-3-chloro-1-(1-naphthalenyloxy)propyl]-

Chemical Property:

Boiling Point:464.9±30.0 °C(Predicted)
PSA：37.47000
Density:1.246±0.06 g/cm3(Predicted)
LogP:5.65030

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Thiophene, 2-[(1S)-3-chloro-1-(1-naphthalenyloxy)propyl]-

There total 1 articles about Thiophene, 2-[(1S)-3-chloro-1-(1-naphthalenyloxy)propyl]- 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:

: 40570-64-7
3-chloro-1-(2-thienyl)propan-1-one

: 164071-61-8
(S)-2-[3-chloro-1-(naphthalen-1-yloxy)-propyl]-thiophene

Guidance literature:: Multi-step reaction with 2 steps

1: (S)-1-Me-3,3-Ph₂-tetrahydro-pyrrolo[1,2-c][1,3,2]oxazaborole; BH₃ / tetrahydrofuran

2: diethylazodicarboxylate; Ph₃P

With borane; triphenylphosphine; (S)-1-methyl-3,3-diphenyl-hexahydropyrrolo[1,2-c][1,3,2]oxazaborole; diethylazodicarboxylate; In tetrahydrofuran; 2: Mitsunobu reaction;
DOI:10.1016/j.bmcl.2003.08.079

Reference yield:

: 164071-61-8
(S)-2-[3-chloro-1-(naphthalen-1-yloxy)-propyl]-thiophene

: 116539-58-3,116539-59-4,116539-60-7,116817-13-1
Duloxetine

Guidance literature:: Multi-step reaction with 2 steps

1: NaI / acetone

2: tetrahydrofuran

With sodium iodide; In tetrahydrofuran; acetone;
DOI:10.1016/j.bmcl.2003.08.079