4,4,5,5-tetramethyl-2-[4-(propan-2-yl)cyclohex-1-en-1-yl]-1,3,2-dioxaborolane

Base Information

Chemical Name:4,4,5,5-tetramethyl-2-[4-(propan-2-yl)cyclohex-1-en-1-yl]-1,3,2-dioxaborolane
CAS No.:1591906-87-4
Molecular Formula:C₁₅H₂₇BO₂
Molecular Weight:250.189
Hs Code.:

Synonyms:4,4,5,5-tetramethyl-2-[4-(propan-2-yl)cyclohex-1-en-1-yl]-1,3,2-dioxaborolane

Suppliers and Price of 4,4,5,5-tetramethyl-2-[4-(propan-2-yl)cyclohex-1-en-1-yl]-1,3,2-dioxaborolane

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

TRC
4,4,5,5-Tetramethyl-2-[4-(1-methylethyl)-1-cyclohexen-1-yl]-1,3,2-dioxaborolane
500mg
$ 165.00

Medical Isotopes, Inc.
4,4,5,5-Tetramethyl-2-[4-(1-methylethyl)-1-cyclohexen-1-yl]-1,3,2-dioxaborolane
500 mg
$ 650.00

Crysdot
2-(4-Isopropylcyclohex-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 95+%
1g
$ 546.00

Chemenu
2-(4-Isopropylcyclohex-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 95+%
1g
$ 555.00

Total 5 raw suppliers

Chemical Property of 4,4,5,5-tetramethyl-2-[4-(propan-2-yl)cyclohex-1-en-1-yl]-1,3,2-dioxaborolane

Chemical Property:

Purity/Quality:

98% ^*data from raw suppliers

4,4,5,5-Tetramethyl-2-[4-(1-methylethyl)-1-cyclohexen-1-yl]-1,3,2-dioxaborolane ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses 4,4,5,5-Tetramethyl-2-[4-(1-methylethyl)-1-cyclohexen-1-yl]-1,3,2-dioxaborolane, is used as a reagent in the synthetic preparation of substituted thienylacetic acids which are inhibitor of viral replication for HIV infection.

Technology Process of 4,4,5,5-tetramethyl-2-[4-(propan-2-yl)cyclohex-1-en-1-yl]-1,3,2-dioxaborolane

There total 3 articles about 4,4,5,5-tetramethyl-2-[4-(propan-2-yl)cyclohex-1-en-1-yl]-1,3,2-dioxaborolane 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:

: 256637-43-1
4-isopropylcyclohex-1-en-1-yl trifluoromethanesulfonate

: 73183-34-3
bis(pinacol)diborane

: 1591906-87-4
4,4,5,5-tetramethyl-2-[4-(propan-2-yl)cyclohex-1-en-1-yl]-1,3,2-dioxaborolane

Guidance literature:: With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate; In 1,4-dioxane; at 80 ℃; for 6h;

Reference yield:

: 4-(propan-2-yl)cyclohex-1-en-1-yl trifluoromethane sulfonate

: 1591906-87-4
4,4,5,5-tetramethyl-2-[4-(propan-2-yl)cyclohex-1-en-1-yl]-1,3,2-dioxaborolane

Guidance literature:: With potassium acetate; In 1,4-dioxane;

Reference yield:

: 5432-85-9
4-isopropyl-cyclohexanone

: 1591906-87-4
4,4,5,5-tetramethyl-2-[4-(propan-2-yl)cyclohex-1-en-1-yl]-1,3,2-dioxaborolane

Guidance literature:: Multi-step reaction with 2 steps

1.1: lithium diisopropyl amide / tetrahydrofuran; n-heptane; ethylbenzene / 1.5 h / -70 °C / Inert atmosphere

1.2: 3 h / -70 °C / Inert atmosphere

2.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate / 1,4-dioxane / 6 h / 80 °C

With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate; lithium diisopropyl amide; In tetrahydrofuran; 1,4-dioxane; n-heptane; ethylbenzene;