trans-2-((2-Hydroxy-1,2,3,4-tetrahydronaphthalene-1-yl)imino)-3-acetylthiazolidine

Base Information

Chemical Name:trans-2-((2-Hydroxy-1,2,3,4-tetrahydronaphthalene-1-yl)imino)-3-acetylthiazolidine
CAS No.:141034-17-5
Molecular Formula:C15H18N2O2S
Molecular Weight:290.3806
Hs Code.:
DSSTox Substance ID:DTXSID60930975
Mol file:141034-17-5.mol

Synonyms:BRN 5351285;trans-2-((2-Hydroxy-1,2,3,4-tetrahydronaphthalene-1-yl)imino)-3-acetylthiazolidine;141034-17-5;2-Thiazolidinimine, 3-acetyl-N-(1,2,3,4-tetrahydro-2-hydroxy-1-naphthalenyl)-, trans-;Ethanone, 1-(1-((2-hydroxy-1,2,3,4-tetrahydro-1-naphthalenyl)imino)-3-thiazolidinyl)-, (E)-;trans-3-Acetyl-N-(1,2,3,4-tetrahydro-2-hydroxy-1-naphthalenyl)-2-thiazolidinimine;DTXSID60930975;LS-151585;1-[3-(2-Hydroxy-1,2,3,4-tetrahydronaphthalen-1-yl)-2-imino-1,3-thiazolidin-5-yl]ethan-1-one

Suppliers and Price of trans-2-((2-Hydroxy-1,2,3,4-tetrahydronaphthalene-1-yl)imino)-3-acetylthiazolidine

Supply Marketing:

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

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Chemical Property of trans-2-((2-Hydroxy-1,2,3,4-tetrahydronaphthalene-1-yl)imino)-3-acetylthiazolidine

Chemical Property:

Vapor Pressure:1.21E-09mmHg at 25°C
Boiling Point:470.2°C at 760 mmHg
Flash Point:238.2°C
Density:1.42g/cm³
XLogP3:1.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:290.10889899
Heavy Atom Count:20
Complexity:415

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)C1CN(C(=N)S1)C2C(CCC3=CC=CC=C23)O
Isomeric SMILES:CC(=O)C1CN(C(=N)S1)[C@H]2[C@@H](CCC3=CC=CC=C23)O

Technology Process of trans-2-((2-Hydroxy-1,2,3,4-tetrahydronaphthalene-1-yl)imino)-3-acetylthiazolidine

There total 4 articles about trans-2-((2-Hydroxy-1,2,3,4-tetrahydronaphthalene-1-yl)imino)-3-acetylthiazolidine 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: 98.0%

: 108-24-7
acetic anhydride

: 141034-15-3
trans-2-iminothiazolidine

: 141034-17-5
trans-2-imino-3-acetyl thiazolidine

Guidance literature:: In methanol; for 7h; Heating;
DOI:10.1135/cccc19920415

Reference yield:

: 7480-36-6,13286-65-2,90874-85-4,128083-88-5
(+/-)-trans-1-amino-2-hydroxy-1,2,3,4-tetrahydronaphthalene

: 141034-17-5
trans-2-imino-3-acetyl thiazolidine

Guidance literature:: Multi-step reaction with 4 steps

1: 80 percent / acetone / 1 h / Heating

2: 84 percent / aq. NaOH / 1 h / Heating

3: 53 percent / ethanol / 36 h / Heating

4: 98 percent / methanol / 7 h / Heating

With sodium hydroxide; In methanol; ethanol; acetone;
DOI:10.1135/cccc19920415

Reference yield:

: 141034-11-9
trans-N-(2-hydroxy-1,2,3,4-tetrahydronaphthalene-1-yl)-N'-benzoyl thiourea

: 141034-17-5
trans-2-imino-3-acetyl thiazolidine

Guidance literature:: Multi-step reaction with 3 steps

1: 84 percent / aq. NaOH / 1 h / Heating

2: 53 percent / ethanol / 36 h / Heating

3: 98 percent / methanol / 7 h / Heating

With sodium hydroxide; In methanol; ethanol;
DOI:10.1135/cccc19920415