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4(tert-Butoxycarbonyl-N-methylamino)-phenylboronic acid is a boronic acid derivative with the molecular formula C14H21BN2O4. It features a substituted phenyl ring and a tert-butoxycarbonyl (Boc) protecting group, making it a versatile compound in the fields of organic synthesis and pharmaceutical research.

945756-49-0

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945756-49-0 Usage

Uses

Used in Organic Synthesis:
4(tert-Butoxycarbonyl-N-methylamino)-phenylboronic acid is used as a building block for the preparation of various biologically active molecules and pharmaceutical agents. Its unique structure allows for the creation of diverse compounds with potential therapeutic properties.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4(tert-Butoxycarbonyl-N-methylamino)-phenylboronic acid is utilized for the development of new drugs. Its ability to form stable complexes with diols makes it a valuable component in the synthesis of bioactive molecules.
Used in the Suzuki-Miyaura Cross-Coupling Reaction:
4(tert-Butoxycarbonyl-N-methylamino)-phenylboronic acid is employed as a key reagent in the Suzuki-Miyaura cross-coupling reaction, a widely used method for the synthesis of aryl compounds. This reaction is essential for the production of various organic compounds, including pharmaceuticals and agrochemicals.
Used in the Development of New Materials:
4(tert-Butoxycarbonyl-N-methylamino)-phenylboronic acid has potential applications in the development of new materials, thanks to its unique chemical properties and reactivity. It can be incorporated into the design and synthesis of advanced materials with specific functions and properties.
Used as a Reagent in Asymmetric Catalysis and Organic Transformations:
4(tert-Butoxycarbonyl-N-methylamino)-phenylboronic acid is also used as a reagent in asymmetric catalysis, a technique crucial for the production of enantiomerically pure compounds. Its application in organic transformations allows for the selective formation of desired products, improving the efficiency and selectivity of chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 945756-49-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,7,5 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 945756-49:
(8*9)+(7*4)+(6*5)+(5*7)+(4*5)+(3*6)+(2*4)+(1*9)=220
220 % 10 = 0
So 945756-49-0 is a valid CAS Registry Number.

945756-49-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]phenyl]boronic acid

1.2 Other means of identification

Product number -
Other names 4-(tert-butoxycarbonyl(methyl)amino)phenylboronic acid

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:945756-49-0 SDS

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