4-(1-(tert-ButoxycarbonylaMino)cyclopropyl)phenylboronic acid

Base Information

Chemical Name:4-(1-(tert-ButoxycarbonylaMino)cyclopropyl)phenylboronic acid
CAS No.:1217500-58-7
Molecular Formula:C14H20BNO4
Molecular Weight:277.128
Hs Code.:2931900090
Mol file:1217500-58-7.mol

Synonyms:4-(1-(tert-ButoxycarbonylaMino)cyclopropyl)phenylboronic acid

Suppliers and Price of 4-(1-(tert-ButoxycarbonylaMino)cyclopropyl)phenylboronic acid

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

Matrix Scientific
(4-(1-((tert-Butoxycarbonyl)amino)-cyclopropyl)phenyl)boronic acid 95+%
1g
$ 1647.00

Matrix Scientific
(4-(1-((tert-Butoxycarbonyl)amino)-cyclopropyl)phenyl)boronic acid 95+%
250mg
$ 756.00

Crysdot
(4-(1-((tert-Butoxycarbonyl)amino)cyclopropyl)phenyl)boronicacid 95+%
1g
$ 424.00

American Custom Chemicals Corporation
(4-(1-((TERT-BUTOXYCARBONYL)AMINO)CYCLOPROPYL)PHENYL)BORONIC ACID 95.00%
1G
$ 660.45

Alichem
(4-(1-((tert-Butoxycarbonyl)amino)cyclopropyl)phenyl)boronicacid
1g
$ 445.12

AK Scientific
4-(1-(tert-Butoxycarbonylamino)cyclopropyl)phenylboronicacid
1g
$ 640.00

Total 11 raw suppliers

Chemical Property of 4-(1-(tert-ButoxycarbonylaMino)cyclopropyl)phenylboronic acid

Chemical Property:

PSA：78.79000
LogP:1.27110
Storage Temp.:under inert gas (nitrogen or Argon) at 2-8°C

Purity/Quality:

97% ^*data from raw suppliers

(4-(1-((tert-Butoxycarbonyl)amino)-cyclopropyl)phenyl)boronic acid 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 4-(1-(tert-ButoxycarbonylaMino)cyclopropyl)phenylboronic acid

There total 2 articles about 4-(1-(tert-ButoxycarbonylaMino)cyclopropyl)phenylboronic acid 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: 82.0%

: 1313441-88-1
tert-butyl N-[1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclopropyl]carbamate

: 1217500-58-7
(4-{1-[(tert-butoxycarbonyl)amino]cyclopropyl}phenyl)boronic acid

Guidance literature:: tert-butyl N-[1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclopropyl]carbamate; With sodium periodate; In tetrahydrofuran; water; at 20 ℃; for 0.5h;

With hydrogenchloride; In tetrahydrofuran; water; at 20 ℃; for 4h;

Reference yield:

: 360773-84-8
tert-butyl [1-(4-bromophenyl)-cyclopropyl]-carbamate

: 1217500-58-7
(4-{1-[(tert-butoxycarbonyl)amino]cyclopropyl}phenyl)boronic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate / dimethyl sulfoxide / 12 h / 70 °C / Inert atmosphere

2.1: sodium periodate / tetrahydrofuran; water / 0.5 h / 20 °C

2.2: 4 h / 20 °C

With sodium periodate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate; In tetrahydrofuran; water; dimethyl sulfoxide;