N-(3-Phenyl-1,2-thiazol-5-yl)thiourea

Base Information

Chemical Name:N-(3-Phenyl-1,2-thiazol-5-yl)thiourea
CAS No.:89335-07-9
Molecular Formula:C₁₀H₉N₃S₂
Molecular Weight:235.334
Hs Code.:
DSSTox Substance ID:DTXSID90527296
Wikidata:Q82396463

Synonyms:89335-07-9;N-(3-Phenyl-1,2-thiazol-5-yl)thiourea;DTXSID90527296

Suppliers and Price of N-(3-Phenyl-1,2-thiazol-5-yl)thiourea

Supply Marketing:

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

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Chemical Property of N-(3-Phenyl-1,2-thiazol-5-yl)thiourea

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:235.02378965
Heavy Atom Count:15
Complexity:229

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NSC(=C2)NC(=S)N

Technology Process of N-(3-Phenyl-1,2-thiazol-5-yl)thiourea

There total 1 articles about N-(3-Phenyl-1,2-thiazol-5-yl)thiourea 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:

: 14208-52-7
5-amino-3-phenylisothiazole

: 89335-07-9
N-(3-phenylisothiazolyl-5)thiourea

Guidance literature:: With benzoyl chloride; Yield given. Multistep reaction; 1.) acetone, refluxed, 30 min.; 2.) 15 min.;

Reference yield: 60.0%

: 79-11-8
chloroacetic acid

: 89335-07-9
N-(3-phenylisothiazolyl-5)thiourea

: 89335-25-1
2-(phenylisothiazolylimino-5)-4-thiazolidinone

Guidance literature:: With sodium acetate; In ethanol; for 6h; Heating;

Reference yield:

: 89335-07-9
N-(3-phenylisothiazolyl-5)thiourea

: 5-Bromo-5-(bromo-phenyl-methyl)-2-[(E)-3-phenyl-isothiazol-5-ylimino]-thiazolidin-4-one

Guidance literature:: Multi-step reaction with 3 steps

1: 60 percent / NaOAc / ethanol / 6 h / Heating

2: ethanol / 4 h / Heating

3: bromine / '''''''''''''''''''''''''''''''''''''''''''''''' / acetic acid / 0 °C

With bromine; sodium acetate; ''''''''''''''''''''''''''''''''''''''''''''''''; In ethanol; acetic acid;