(R,Z)-2-(4-((3-(carboxymethyl)-4-oxo-2-thioxothiazolidin-5-ylidene)methyl)benzamido)pentanedioic acid

Base Information

Chemical Name:(R,Z)-2-(4-((3-(carboxymethyl)-4-oxo-2-thioxothiazolidin-5-ylidene)methyl)benzamido)pentanedioic acid
CAS No.:1334590-89-4
Molecular Formula:C₁₈H₁₆N₂O₈S₂
Molecular Weight:452.466
Hs Code.:

Synonyms:(R,Z)-2-(4-((3-(carboxymethyl)-4-oxo-2-thioxothiazolidin-5-ylidene)methyl)benzamido)pentanedioic acid

Suppliers and Price of (R,Z)-2-(4-((3-(carboxymethyl)-4-oxo-2-thioxothiazolidin-5-ylidene)methyl)benzamido)pentanedioic 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 (R,Z)-2-(4-((3-(carboxymethyl)-4-oxo-2-thioxothiazolidin-5-ylidene)methyl)benzamido)pentanedioic acid

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R,Z)-2-(4-((3-(carboxymethyl)-4-oxo-2-thioxothiazolidin-5-ylidene)methyl)benzamido)pentanedioic acid

There total 3 articles about (R,Z)-2-(4-((3-(carboxymethyl)-4-oxo-2-thioxothiazolidin-5-ylidene)methyl)benzamido)pentanedioic 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: 29.0%

: 5718-83-2
rhodanine 3-acetic acid

: 1334590-86-1
(R)-2-(4-formylbenzamido)pentanedioic acid

: 1334590-89-4
(R,Z)-2-(4-((3-(carboxymethyl)-4-oxo-2-thioxothiazolidin-5-ylidene)methyl)benzamido)pentanedioic acid

Guidance literature:: With piperidine; acetic acid; In ethanol; at 150 ℃; for 0.333333h; Microwave irradiation;
DOI:10.1016/j.ejmech.2011.05.070

Reference yield:

: 619-66-9
4-Carboxybenzaldehyde

: 1334590-89-4
(R,Z)-2-(4-((3-(carboxymethyl)-4-oxo-2-thioxothiazolidin-5-ylidene)methyl)benzamido)pentanedioic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 24 h / 20 °C

2.1: lithium hydroxide / methanol; water / 15 h / 20 °C

2.2: pH 2

3.1: piperidine; acetic acid / ethanol / 0.33 h / 150 °C / Microwave irradiation

With piperidine; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; lithium hydroxide; In methanol; ethanol; water; N,N-dimethyl-formamide; 3.1: Knoevenagel condensation;
DOI:10.1016/j.ejmech.2011.05.070

Reference yield:

: 13515-99-6,23150-65-4,27025-25-8
D-glutamic acid dimethyl ester hydrochloride

: 1334590-89-4
(R,Z)-2-(4-((3-(carboxymethyl)-4-oxo-2-thioxothiazolidin-5-ylidene)methyl)benzamido)pentanedioic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 24 h / 20 °C

2.1: lithium hydroxide / methanol; water / 15 h / 20 °C

2.2: pH 2

3.1: piperidine; acetic acid / ethanol / 0.33 h / 150 °C / Microwave irradiation

With piperidine; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; lithium hydroxide; In methanol; ethanol; water; N,N-dimethyl-formamide; 3.1: Knoevenagel condensation;
DOI:10.1016/j.ejmech.2011.05.070