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330793-01-6

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330793-01-6 Usage

Chemical Properties

White crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 330793-01-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,0,7,9 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 330793-01:
(8*3)+(7*3)+(6*0)+(5*7)+(4*9)+(3*3)+(2*0)+(1*1)=126
126 % 10 = 6
So 330793-01-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H28BNO4/c1-16(2,3)22-15(21)20(8)14-11-9-13(10-12-14)19-23-17(4,5)18(6,7)24-19/h9-12H,1-8H3

330793-01-6 Well-known Company Product Price

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  • Alfa Aesar

  • (L19653)  4-(Boc-amino)benzeneboronic acid pinacol ester, 97%   

  • 330793-01-6

  • 1g

  • 691.0CNY

  • Detail
  • Alfa Aesar

  • (L19653)  4-(Boc-amino)benzeneboronic acid pinacol ester, 97%   

  • 330793-01-6

  • 5g

  • 3017.0CNY

  • Detail
  • Aldrich

  • (562351)  4-(N-Boc-amino)phenylboronicacidpinacolester  97%

  • 330793-01-6

  • 562351-1G

  • 800.28CNY

  • Detail
  • Aldrich

  • (562351)  4-(N-Boc-amino)phenylboronicacidpinacolester  97%

  • 330793-01-6

  • 562351-5G

  • 3,304.08CNY

  • Detail

330793-01-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate

1.2 Other means of identification

Product number -
Other names 4-(Boc-amino)benzeneboronic acid pinacol ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:330793-01-6 SDS

330793-01-6Relevant articles and documents

Cooperative Self-Assembly of Pyridine-2,6-Diimine-Linked Macrocycles into Mechanically Robust Nanotubes

Strauss, Michael J.,Asheghali, Darya,Evans, Austin M.,Li, Rebecca L.,Chavez, Anton D.,Sun, Chao,Becker, Matthew L.,Dichtel, William R.

, p. 14708 - 14714 (2019)

Nanotubes assembled from macrocyclic precursors offer a unique combination of low dimensionality, structural rigidity, and distinct interior and exterior microenvironments. Usually the weak stacking energies of macrocycles limit the length and mechanical

Non-innocent Radical Ion Intermediates in Photoredox Catalysis: Parallel Reduction Modes Enable Coupling of Diverse Aryl Chlorides

Chernowsky, Colleen P.,Chmiel, Alyah F.,Wickens, Zachary K.,Williams, Oliver P.,Yeung, Charles S.

supporting information, p. 10882 - 10889 (2021/07/31)

We describe a photocatalytic system that elicits potent photoreductant activity from conventional photocatalysts by leveraging radical anion intermediates generated in situ. The combination of an isophthalonitrile photocatalyst and sodium formate promotes diverse aryl radical coupling reactions from abundant but difficult to reduce aryl chloride substrates. Mechanistic studies reveal two parallel pathways for substrate reduction both enabled by a key terminal reductant byproduct, carbon dioxide radical anion.

Visible Light-Induced Borylation of C-O, C-N, and C-X Bonds

Arman, Hadi D.,Dang, Hang. T.,Haug, Graham C.,He, Ru,Jin, Shengfei,Larionov, Oleg V.,Nguyen, Viet D.,Nguyen, Vu T.,Schanze, Kirk S.

, (2020/02/04)

Boronic acids are centrally important functional motifs and synthetic precursors. Visible light-induced borylation may provide access to structurally diverse boronates, but a broadly efficient photocatalytic borylation method that can effect borylation of a wide range of substrates, including strong C-O bonds, remains elusive. Herein, we report a general, metal-free visible light-induced photocatalytic borylation platform that enables borylation of electron-rich derivatives of phenols and anilines, chloroarenes, as well as other haloarenes. The reaction exhibits excellent functional group tolerance, as demonstrated by the borylation of a range of structurally complex substrates. Remarkably, the reaction is catalyzed by phenothiazine, a simple organic photocatalyst with MW 200 that mediates the previously unachievable visible light-induced single electron reduction of phenol derivatives with reduction potentials as negative as approximately - 3 V versus SCE by a proton-coupled electron transfer mechanism. Mechanistic studies point to the crucial role of the photocatalyst-base interaction.

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