Thiazolo(3,2-b)(1,2,4)triazol-6(5H)-one, 5-((4-chlorophenyl)methylene)-2-phenyl-, (5E)-

Base Information

Chemical Name:Thiazolo(3,2-b)(1,2,4)triazol-6(5H)-one, 5-((4-chlorophenyl)methylene)-2-phenyl-, (5E)-
CAS No.:58755-11-6
Molecular Formula:C₁₇H₁₀ClN₃OS
Molecular Weight:339.805
Hs Code.:

Synonyms:58755-11-6;Thiazolo(3,2-b)(1,2,4)triazol-6(5H)-one, 5-((4-chlorophenyl)methylene)-2-phenyl-, (5E)-;NSC 282760;(5E)-5-[(4-chlorophenyl)methylidene]-2-phenyl-[1,3]thiazolo[3,2-b][1,2,4]triazol-6-one;NSC282760;Thiazolo[3,2-b][1,2,4]triazol-6(5H)-one, 5-[(4-chlorophenyl)methylene]-2-phenyl-, (5E)-;STK815093;AKOS002194301;(5E)-5-(4-chlorobenzylidene)-2-phenyl[1,3]thiazolo[3,2-b][1,2,4]triazol-6(5H)-one;(5E)-5-[(4-chlorophenyl)methylene]-2-phenyl-thiazolo[3,2-b][1,2,4]triazol-6-one;5-(4-CHLOROBENZYLIDENE)-2-PHENYL(1,3)THIAZOLO(3,2-B)(1,2,4)TRIAZOL-6(5H)-ONE

Suppliers and Price of Thiazolo(3,2-b)(1,2,4)triazol-6(5H)-one, 5-((4-chlorophenyl)methylene)-2-phenyl-, (5E)-

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 2 raw suppliers

Chemical Property of Thiazolo(3,2-b)(1,2,4)triazol-6(5H)-one, 5-((4-chlorophenyl)methylene)-2-phenyl-, (5E)-

Chemical Property:

Vapor Pressure:8.58E-13mmHg at 25°C
Boiling Point:565.1°C at 760 mmHg
Flash Point:295.6°C
Density:1.45g/cm³
XLogP3:4.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:339.0233108
Heavy Atom Count:23
Complexity:486

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NN3C(=O)C(=CC4=CC=C(C=C4)Cl)SC3=N2
Isomeric SMILES:C1=CC=C(C=C1)C2=NN3C(=O)/C(=C\C4=CC=C(C=C4)Cl)/SC3=N2

Technology Process of Thiazolo(3,2-b)(1,2,4)triazol-6(5H)-one, 5-((4-chlorophenyl)methylene)-2-phenyl-, (5E)-

There total 3 articles about Thiazolo(3,2-b)(1,2,4)triazol-6(5H)-one, 5-((4-chlorophenyl)methylene)-2-phenyl-, (5E)- 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:

: 5351-66-6
benzoyl thiosemicarbazide

: 58755-11-6
5-(4-chloro-benzylidene)-2-phenyl-thiazolo[3,2-b][1,2,4]triazol-6-one

Guidance literature:: Multi-step reaction with 2 steps

1: aq. KOH (10 percent) / 3 h / Heating

2: 10.4 percent / Ac₂O; NaOCOCH₃ / acetic acid / 6 h / Heating

With potassium hydroxide; sodium acetate; acetic anhydride; In acetic acid; 1: Cyclization / 2: Cyclization;

Reference yield:

: 98-88-4
benzoyl chloride

: 58755-11-6
5-(4-chloro-benzylidene)-2-phenyl-thiazolo[3,2-b][1,2,4]triazol-6-one

Guidance literature:: Multi-step reaction with 3 steps

1: propan-2-ol / 2 h / Heating

2: aq. KOH (10 percent) / 3 h / Heating

3: 10.4 percent / Ac₂O; NaOCOCH₃ / acetic acid / 6 h / Heating

With potassium hydroxide; sodium acetate; acetic anhydride; In acetic acid; isopropyl alcohol; 1: Acylation / 2: Cyclization / 3: Cyclization;

Reference yield:

: 58755-01-4
<(3-Phenyl-1,2,4-triazolo-5-yl)thio>essigsaeure

: 58755-11-6
5-(4-chloro-benzylidene)-2-phenyl-thiazolo[3,2-b][1,2,4]triazol-6-one

Guidance literature:: Multi-step reaction with 2 steps

1: Ac₂O / Heating

2: acetic anhydride / Heating

With acetic anhydride; In acetic anhydride;