Benzamide, N-(((2-hydroxy-1,2,3,4-tetrahydro-1-naphthalenyl)amino)thioxomethyl)-, (E)-

Base Information

Chemical Name:Benzamide, N-(((2-hydroxy-1,2,3,4-tetrahydro-1-naphthalenyl)amino)thioxomethyl)-, (E)-
CAS No.:141034-11-9
Molecular Formula:C₁₈H₁₈N₂O₂S
Molecular Weight:326.419
Hs Code.:
DSSTox Substance ID:DTXSID40161528
Wikidata:Q76278648

Synonyms:BRN 5351481;Benzamide, N-(((2-hydroxy-1,2,3,4-tetrahydro-1-naphthalenyl)amino)thioxomethyl)-, (E)-;trans-N-(2-Hydroxy-1,2,3,4-tetrahydronaphthalene-1-yl)-N'-benzoylthiourea;N-(((2-Hydroxy-1,2,3,4-tetrahydro-1-naphthalenyl)amino)thioxomethyl)benzamide (E)-;141034-11-9;DTXSID40161528;LS-27022

Suppliers and Price of Benzamide, N-(((2-hydroxy-1,2,3,4-tetrahydro-1-naphthalenyl)amino)thioxomethyl)-, (E)-

Supply Marketing:

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

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Chemical Property of Benzamide, N-(((2-hydroxy-1,2,3,4-tetrahydro-1-naphthalenyl)amino)thioxomethyl)-, (E)-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.33g/cm³
XLogP3:3.3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:326.10889899
Heavy Atom Count:23
Complexity:437

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC2=CC=CC=C2C(C1O)NC(=S)NC(=O)C3=CC=CC=C3
Isomeric SMILES:C1CC2=CC=CC=C2[C@H]([C@@H]1O)NC(=S)NC(=O)C3=CC=CC=C3

Technology Process of Benzamide, N-(((2-hydroxy-1,2,3,4-tetrahydro-1-naphthalenyl)amino)thioxomethyl)-, (E)-

There total 1 articles about Benzamide, N-(((2-hydroxy-1,2,3,4-tetrahydro-1-naphthalenyl)amino)thioxomethyl)-, (E)- 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: 80.0%

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

: 532-55-8
Benzoyl isothiocyanate

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

Guidance literature:: In acetone; for 1h; Heating;
DOI:10.1135/cccc19920415

Reference yield: 84.0%

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

: 141034-13-1
trans-N-(2-hydroxy-1,2,3,4-tetrahydronaphthalene-1-yl) thiourea

Guidance literature:: With sodium hydroxide; for 1h; Heating;
DOI:10.1135/cccc19920415

Reference yield:

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

: 141034-15-3
trans-2-iminothiazolidine

Guidance literature:: Multi-step reaction with 2 steps

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

2: 53 percent / ethanol / 36 h / Heating

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