C₅₁H₅₈N₄O₂S₃

Base Information

Chemical Name:C₅₁H₅₈N₄O₂S₃
CAS No.:1416172-57-0
Molecular Formula:C₅₁H₅₈N₄O₂S₃
Molecular Weight:855.245
Hs Code.:

C<sub>51</sub>H<sub>58</sub>N<sub>4</sub>O<sub>2</sub>S<sub>3</sub>

Synonyms:C₅₁H₅₈N₄O₂S₃

Suppliers and Price of C₅₁H₅₈N₄O₂S₃

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 C₅₁H₅₈N₄O₂S₃

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₅₁H₅₈N₄O₂S₃

There total 5 articles about C₅₁H₅₈N₄O₂S₃ 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: 65.0%

: 1416172-52-5
5-(4,4'-dinonyl-5'-(4-(phenyl(p-tolyl)amino)phenyl)-2,2'-bithiazol-5-yl)thiophene-2-carbaldehyde

: 372-09-8
cyanoacetic acid

: 1416172-57-0
C₅₁H₅₈N₄O₂S₃

Guidance literature:: With piperidine; In chloroform; Inert atmosphere; Schlenk technique; Reflux;
DOI:10.1016/j.dyepig.2012.10.002

Reference yield:

: 98-03-3
thiophene-2-carbaldehyde

: 1416172-57-0
C₅₁H₅₈N₄O₂S₃

Guidance literature:: Multi-step reaction with 6 steps

1: toluene-4-sulfonic acid / benzene / Inert atmosphere; Schlenk technique

2: Trimethyl borate; hydrogenchloride; n-butyllithium / water / Inert atmosphere; Schlenk technique

3: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate / tetrahydrofuran; water / 48 h / 80 °C / Inert atmosphere; Schlenk technique

4: N-Bromosuccinimide; acetic acid / chloroform / Inert atmosphere; Schlenk technique

5: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate / tetrahydrofuran; water / Inert atmosphere; Schlenk technique

6: piperidine / chloroform / Inert atmosphere; Schlenk technique; Reflux

With piperidine; hydrogenchloride; N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; n-butyllithium; Trimethyl borate; sodium carbonate; toluene-4-sulfonic acid; acetic acid; In tetrahydrofuran; chloroform; water; benzene; 3: |Suzuki Coupling / 5: |Suzuki Coupling / 6: |Knoevenagel Condensation;
DOI:10.1016/j.dyepig.2012.10.002

Reference yield:

: 58268-08-9
2-(2-thienyl)-1,3-dioxolane

: 1416172-57-0
C₅₁H₅₈N₄O₂S₃

Guidance literature:: Multi-step reaction with 5 steps

1: Trimethyl borate; hydrogenchloride; n-butyllithium / water / Inert atmosphere; Schlenk technique

2: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate / tetrahydrofuran; water / 48 h / 80 °C / Inert atmosphere; Schlenk technique

3: N-Bromosuccinimide; acetic acid / chloroform / Inert atmosphere; Schlenk technique

4: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate / tetrahydrofuran; water / Inert atmosphere; Schlenk technique

5: piperidine / chloroform / Inert atmosphere; Schlenk technique; Reflux

With piperidine; hydrogenchloride; N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; n-butyllithium; Trimethyl borate; sodium carbonate; acetic acid; In tetrahydrofuran; chloroform; water; 2: |Suzuki Coupling / 4: |Suzuki Coupling / 5: |Knoevenagel Condensation;
DOI:10.1016/j.dyepig.2012.10.002