C₂HF₃O₂*C₃₉H₅₂N₄O₁₀S₂

Base Information

Chemical Name:C₂HF₃O₂*C₃₉H₅₂N₄O₁₀S₂
CAS No.:1392236-23-5
Molecular Formula:C₂HF₃O₂*C₃₉H₅₂N₄O₁₀S₂
Molecular Weight:915.019
Hs Code.:

C<sub>2</sub>HF<sub>3</sub>O<sub>2</sub>*C<sub>39</sub>H<sub>52</sub>N<sub>4</sub>O<sub>10</sub>S<sub>2</sub>

Synonyms:

Suppliers and Price of C₂HF₃O₂*C₃₉H₅₂N₄O₁₀S₂

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 C₂HF₃O₂*C₃₉H₅₂N₄O₁₀S₂

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂HF₃O₂*C₃₉H₅₂N₄O₁₀S₂

There total 13 articles about C₂HF₃O₂*C₃₉H₅₂N₄O₁₀S₂ 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:

: BrH*C₁₀H₂₅N₃O₃S

: C₃₃H₃₂N₂O₁₀S

: 76-05-1
trifluoroacetic acid

: 1392236-23-5
C₂HF₃O₂*C₃₉H₅₂N₄O₁₀S₂

Guidance literature:: BrH*C₁₀H₂₅N₃O₃S; C₃₃H₃₂N₂O₁₀S; With sodium hydrogencarbonate; In water; N,N-dimethyl-formamide; at 20 ℃; for 0.5h;

trifluoroacetic acid; In water; N,N-dimethyl-formamide;
DOI:10.1039/c2ob00022a

Reference yield:

: 1286282-27-6
2',6'-dimethyl-4'-methoxycarbonylphenyl 2-isopropyloxyacridine-9-carboxylate

: 1392236-23-5
C₂HF₃O₂*C₃₉H₅₂N₄O₁₀S₂

Guidance literature:: Multi-step reaction with 4 steps

1: 2,6-di-tert-butyl-pyridine / 16 h / 155 °C / Inert atmosphere; Ionic liquid

2: hydrogenchloride / water / 3 h / Reflux; Inert atmosphere

3: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.25 h / 20 °C

4: sodium hydrogencarbonate / water; N,N-dimethyl-formamide / 0.5 h / 20 °C

With hydrogenchloride; 2,6-di-tert-butyl-pyridine; sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; In water; N,N-dimethyl-formamide;
DOI:10.1039/c2ob00022a

Reference yield:

: 130266-57-8
2-methoxyacridine-9-carboxylic acid

: 1392236-23-5
C₂HF₃O₂*C₃₉H₅₂N₄O₁₀S₂

Guidance literature:: Multi-step reaction with 7 steps

1.1: pyridine; p-toluenesulfonyl chloride / 4 h / 20 °C / Inert atmosphere

2.1: boron tribromide / dichloromethane / 4 h / 20 °C

2.2: 16 h / 0 - 20 °C

3.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 1 h / 0 °C / Inert atmosphere

4.1: 2,6-di-tert-butyl-pyridine / 16 h / 155 °C / Inert atmosphere; Ionic liquid

5.1: hydrogenchloride / water / 3 h / Reflux; Inert atmosphere

6.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.25 h / 20 °C

7.1: sodium hydrogencarbonate / water; N,N-dimethyl-formamide / 0.5 h / 20 °C

With pyridine; hydrogenchloride; 2,6-di-tert-butyl-pyridine; di-isopropyl azodicarboxylate; boron tribromide; sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; p-toluenesulfonyl chloride; triphenylphosphine; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; 3.1: Mitsunobu reaction;
DOI:10.1039/c2ob00022a