N-(4-(5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-4-oxothiazolidin-2-ylideneamino)phenyl)oxalamic acid

Base Information

Chemical Name:N-(4-(5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-4-oxothiazolidin-2-ylideneamino)phenyl)oxalamic acid
CAS No.:1186633-83-9
Molecular Formula:C₃₂H₃₁N₃O₅S
Molecular Weight:569.681
Hs Code.:

Synonyms:N-(4-(5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-4-oxothiazolidin-2-ylideneamino)phenyl)oxalamic acid

Suppliers and Price of N-(4-(5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-4-oxothiazolidin-2-ylideneamino)phenyl)oxalamic acid

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
Packaging
price

Total 0 raw suppliers

Chemical Property of N-(4-(5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-4-oxothiazolidin-2-ylideneamino)phenyl)oxalamic acid

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-(4-(5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-4-oxothiazolidin-2-ylideneamino)phenyl)oxalamic acid

There total 9 articles about N-(4-(5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-4-oxothiazolidin-2-ylideneamino)phenyl)oxalamic acid 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: 88.0%

: 1186634-20-7
N-(4-(5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-4-oxothiazolidin-2-ylideneamino)phenyl)oxalamic acid ethyl ester

: 1186633-83-9
N-(4-(5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-4-oxothiazolidin-2-ylideneamino)phenyl)oxalamic acid

Guidance literature:: N-(4-(5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-4-oxothiazolidin-2-ylideneamino)phenyl)oxalamic acid ethyl ester; With water; lithium hydroxide; In tetrahydrofuran; methanol; at 20 ℃; for 3h;

With hydrogenchloride; In water; pH=4;

Reference yield:

: 63500-84-5
3-methyl-2-(4-nitro-phenylimino)-thiazolidin-4-one

: 1186633-83-9
N-(4-(5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-4-oxothiazolidin-2-ylideneamino)phenyl)oxalamic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: piperidine / ethanol / 14 h / Reflux

2.1: iron; acetic acid / 6 h / 20 °C

3.1: triethylamine / dichloromethane / 0 - 20 °C

4.1: water; lithium hydroxide / tetrahydrofuran; methanol / 3 h / 20 °C

4.2: pH 4

With piperidine; water; iron; acetic acid; triethylamine; lithium hydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane;

Reference yield:

: 1186634-26-3
4-(4-cyclohexylbenzyloxy)benzaldehyde

: 1186633-83-9
N-(4-(5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-4-oxothiazolidin-2-ylideneamino)phenyl)oxalamic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: piperidine / ethanol / 14 h / Reflux

2.1: iron; acetic acid / 6 h / 20 °C

3.1: triethylamine / dichloromethane / 0 - 20 °C

4.1: water; lithium hydroxide / tetrahydrofuran; methanol / 3 h / 20 °C

4.2: pH 4

With piperidine; water; iron; acetic acid; triethylamine; lithium hydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane;