4,5-dimethyl-N,3-diphenyl-1,3-thiazol-2-imine

Base Information

• Chemical Name: 4,5-dimethyl-N,3-diphenyl-1,3-thiazol-2-imine
• CAS No.: 82694-43-7
• Molecular Formula: C₁₇H₁₆N₂S
• Molecular Weight: 280.393
• Hs Code.: 2934100090
• DSSTox Substance ID: DTXSID40384038
• Mol file: 82694-43-7.mol

Synonyms:82694-43-7;4,5-dimethyl-N,3-diphenyl-1,3-thiazol-2-imine;(4,5-Dimethyl-3-phenyl-3H-thiazol-2-ylidene)-phenyl-amine;DTXSID40384038;CCG-244027

Chemical Property of 4,5-dimethyl-N,3-diphenyl-1,3-thiazol-2-imine

Chemical Property:

• PSA: 45.53000
• LogP: 4.38800
• XLogP3: 4.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 280.10341969
• Heavy Atom Count: 20
• Complexity: 401

Purity/Quality:

(4,5-DIMETHYL-3-PHENYL-3H-THIAZOL-2-YLIDENE)-PHENYL-AMINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(SC(=NC2=CC=CC=C2)N1C3=CC=CC=C3)C

Technology Process of 4,5-dimethyl-N,3-diphenyl-1,3-thiazol-2-imine

There total 5 articles about 4,5-dimethyl-N,3-diphenyl-1,3-thiazol-2-imine 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: 69.0%

N,N-diphenylthiourea (102-08-9) + 3-bromo-butanone (814-75-5) → (4,5-dimethyl-3-phenyl-3H-thiazol-2-ylidene)-phenyl-amine (82694-43-7)

Guidance literature:

With triethylamine; In acetonitrile; at 60 ℃; for 1.5h;

DOI:10.1016/j.tet.2007.11.076

Reference yield:

1,1-diphenylthiourea (3898-08-6) + butanone (78-93-3) → (4,5-dimethyl-3-phenyl-3H-thiazol-2-ylidene)-phenyl-amine (82694-43-7)

Guidance literature:

With iodine;

Reference yield:

N,N-diphenylthiourea (102-08-9) + butanone (78-93-3) → (4,5-dimethyl-3-phenyl-3H-thiazol-2-ylidene)-phenyl-amine (82694-43-7)

Guidance literature:

With bromine; Multistep reaction; 1. benzene, 2. reflux;

upstream raw materials:

1,1-diphenylthiourea

3-chloro-2-butanone

3-mercapto-2-butanone

1,3-Diphenylcarbodiimide