C₇H₅BF₅^(1-)*K⁽¹⁺⁾

Base Information

Chemical Name:C₇H₅BF₅^(1-)*K⁽¹⁺⁾
CAS No.:1632070-90-6
Molecular Formula:C₇H₅BF₅*K
Molecular Weight:234.018
Hs Code.:

C<sub>7</sub>H<sub>5</sub>BF<sub>5</sub><sup>(1-)</sup>*K<sup>(1+)</sup>

Synonyms:C₇H₅BF₅^(1-)*K⁽¹⁺⁾

Suppliers and Price of C₇H₅BF₅^(1-)*K⁽¹⁺⁾

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 2 raw suppliers

Chemical Property of C₇H₅BF₅^(1-)*K⁽¹⁺⁾

Chemical Property:

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

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Technology Process of C₇H₅BF₅^(1-)*K⁽¹⁺⁾

There total 1 articles about C₇H₅BF₅^(1-)*K⁽¹⁺⁾ 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: 76.0%

: potassium hydrogen difluoride

: 23915-07-3
1-(bromomethyl)-2,4-difluorobenzene

: 73183-34-3
bis(pinacol)diborane

: 1632070-90-6
C₇H₅BF₅^(1-)*K⁽¹⁺⁾

Guidance literature:: 1-(bromomethyl)-2,4-difluorobenzene; bis(pinacol)diborane; With copper(l) iodide; lithium methanolate; triphenylphosphine; In N,N-dimethyl-formamide; at 20 ℃; for 20h; Inert atmosphere;

potassium hydrogen difluoride; In methanol; ethyl acetate; at 0 - 20 ℃; for 1.5h; Inert atmosphere;
DOI:10.1002/anie.201700097

Reference yield: 96.0%

: 1632070-90-6
C₇H₅BF₅^(1-)*K⁽¹⁺⁾

: 150256-91-0
ethyl 5-methylbenzo[d]isothiazole-3-carboxylate 1,1-dioxide

: C₁₇H₁₅F₂NO₄S

Guidance literature:: With copper(II) tetrafluoroborate monohydrate; C₅₃H₅₈N₂O₂; In chloroform; at -20 ℃; for 12h; enantioselective reaction; Inert atmosphere; Schlenk technique; Irradiation;
DOI:10.1021/jacs.8b09251

Reference yield: 76.0%

: 941-55-9
4-toluenesulfonyl azide

: 1632070-90-6
C₇H₅BF₅^(1-)*K⁽¹⁺⁾

: C₁₄H₁₃F₂NO₂S

Guidance literature:: With tris(2,2-bipyridine)ruthenium(II) hexafluorophosphate; (1,2-dimethoxyethane)dichloronickel(II); dimethylglyoxal; In acetonitrile; at 20 ℃; for 24h; Inert atmosphere; Irradiation;
DOI:10.1021/acscatal.1c00731