C₁₄H₁₆F₂N₂O₃*ClH

Base Information

Chemical Name:C₁₄H₁₆F₂N₂O₃*ClH
CAS No.:1574285-43-0
Molecular Formula:C₁₄H₁₆F₂N₂O₃*ClH
Molecular Weight:334.75
Hs Code.:

C<sub>14</sub>H<sub>16</sub>F<sub>2</sub>N<sub>2</sub>O<sub>3</sub>*ClH

Synonyms:C₁₄H₁₆F₂N₂O₃*ClH

Suppliers and Price of C₁₄H₁₆F₂N₂O₃*ClH

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 1 raw suppliers

Chemical Property of C₁₄H₁₆F₂N₂O₃*ClH

Chemical Property:

Purity/Quality:: 98% ,99% , ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₁₄H₁₆F₂N₂O₃*ClH

There total 16 articles about C₁₄H₁₆F₂N₂O₃*ClH 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: 100.0%

: 1574285-40-7
2-((2-(4-difluoromethoxy-3-isopropoxyphenyl)oxazol-4-yl)methyl)isoindoline-1,3-dione

: 1574285-43-0
C₁₄H₁₆F₂N₂O₃*ClH

Guidance literature:: 2-((2-(4-difluoromethoxy-3-isopropoxyphenyl)oxazol-4-yl)methyl)isoindoline-1,3-dione; With methylamine; In methanol; water; for 0.5h; Reflux;

With cyclopentyl methyl ether; sodium hydroxide; In methanol; water; at 65 - 75 ℃;

With hydrogenchloride; In methanol; water;

Reference yield:

: 159783-48-9
4-Difluoromethoxy-3-(1-methyl)ethoxybenzoic acid

: 1574285-43-0
C₁₄H₁₆F₂N₂O₃*ClH

Guidance literature:: Multi-step reaction with 5 steps

1.1: 1,1'-carbonyldiimidazole / acetonitrile / 1 h / 20 °C

1.2: 2 h / 0 °C

2.1: 3-chloro-2-oxopropyl acetate / toluene / 22 h / Molecular sieve; Reflux

2.2: 0.25 h / Reflux

3.1: triethylamine; methanesulfonyl chloride / ethyl acetate / 1 h / 20 °C

3.2: 1 h / 30 °C

4.1: N,N-dimethyl-formamide / 1 h / 80 °C

5.1: methylamine / water; methanol / 0.5 h / Reflux

With 3-chloro-2-oxopropyl acetate; methanesulfonyl chloride; triethylamine; 1,1'-carbonyldiimidazole; methylamine; In methanol; water; ethyl acetate; N,N-dimethyl-formamide; toluene; acetonitrile;

Reference yield:

: 1574285-91-8
C₁₁H₁₃F₂NO₃

: 1574285-43-0
C₁₄H₁₆F₂N₂O₃*ClH

Guidance literature:: Multi-step reaction with 4 steps

1.1: 3-chloro-2-oxopropyl acetate / toluene / 22 h / Molecular sieve; Reflux

1.2: 0.25 h / Reflux

2.1: triethylamine; methanesulfonyl chloride / ethyl acetate / 1 h / 20 °C

2.2: 1 h / 30 °C

3.1: N,N-dimethyl-formamide / 1 h / 80 °C

4.1: methylamine / water; methanol / 0.5 h / Reflux

With 3-chloro-2-oxopropyl acetate; methanesulfonyl chloride; triethylamine; methylamine; In methanol; water; ethyl acetate; N,N-dimethyl-formamide; toluene;