1H-Inden-2-ol, 2,3-dihydro-1-((4,5-dihydro-2-thiazolyl)amino)-, trans-

Base Information

Chemical Name:1H-Inden-2-ol, 2,3-dihydro-1-((4,5-dihydro-2-thiazolyl)amino)-, trans-
CAS No.:141034-16-4
Molecular Formula:C12H14N2OS
Molecular Weight:234.3174
Hs Code.:
DSSTox Substance ID:DTXSID30161532
Wikidata:Q76278666
Mol file:141034-16-4.mol

Synonyms:BRN 5341103;trans-2-(N-(2-Hydroxyindan-1-yl)imino)thiazolidine;1H-Inden-2-ol, 2,3-dihydro-1-((4,5-dihydro-2-thiazolyl)amino)-, trans-;1H-Inden-2-ol, 2,3-dihydro-1-(2-thiazolidinylideneamino)-, (E)-;trans-2,3-Dihydro-1-((4,5-dihydro-2-thiazolyl)amino)-1H-inden-2-ol;141034-16-4;DTXSID30161532;LS-81788

Suppliers and Price of 1H-Inden-2-ol, 2,3-dihydro-1-((4,5-dihydro-2-thiazolyl)amino)-, trans-

Supply Marketing:

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

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Chemical Property of 1H-Inden-2-ol, 2,3-dihydro-1-((4,5-dihydro-2-thiazolyl)amino)-, trans-

Chemical Property:

Vapor Pressure:8.64E-08mmHg at 25°C
Boiling Point:419.6°Cat760mmHg
Flash Point:207.5°C
Density:1.45g/cm³
XLogP3:1.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:234.08268425
Heavy Atom Count:16
Complexity:295

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CSC(=N1)NC2C(CC3=CC=CC=C23)O
Isomeric SMILES:C1CSC(=N1)N[C@H]2[C@@H](CC3=CC=CC=C23)O

Technology Process of 1H-Inden-2-ol, 2,3-dihydro-1-((4,5-dihydro-2-thiazolyl)amino)-, trans-

There total 3 articles about 1H-Inden-2-ol, 2,3-dihydro-1-((4,5-dihydro-2-thiazolyl)amino)-, trans- 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: 56.0%

: 2576-47-8
2-bromoethylamine hydrobromide

: 141034-14-2
trans-N-(2-hydroxyindane-1-yl) thiourea

: 141034-16-4
trans-2-iminothiazolidine

Guidance literature:: In ethanol; for 36h; Heating;
DOI:10.1135/cccc19920415

Reference yield:

: 7480-35-5,13286-59-4,74165-73-4,126456-43-7,136030-00-7,140632-19-5,140632-20-8
trans-1-aminoindan-2-ol

: 141034-16-4
trans-2-iminothiazolidine

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / acetone / 1 h / Heating

2: 76 percent / aq. NaOH / 1 h / Heating

3: 56 percent / ethanol / 36 h / Heating

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

Reference yield:

: 141034-12-0
trans-N-(2-hydroxyindane-1-yl)-N'-benzoyl thiourea

: 141034-16-4
trans-2-iminothiazolidine

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / aq. NaOH / 1 h / Heating

2: 56 percent / ethanol / 36 h / Heating

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