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(4-Benzyloxycarbonylaminophenyl)boronic acid, pinacol ester is an organic compound and a boronic acid derivative, specifically the pinacol ester of (4-Benzyloxycarbonylaminophenyl)boronic acid. It is characterized by its role in various chemical reactions and synthesis processes, particularly in the formation of carbon-carbon bonds and the synthesis of complex organic molecules. This makes it a valuable reagent in pharmaceutical and agrochemical research.

363186-06-5

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363186-06-5 Usage

Uses

Used in Pharmaceutical and Agrochemical Research:
(4-Benzyloxycarbonylaminophenyl)boronic acid, pinacol ester is used as a reagent in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules. It is instrumental in the development of new drug candidates and fine chemical production due to its ability to facilitate the formation of carbon-carbon bonds, which are crucial in the creation of diverse molecular structures.
Used in Chemical Reactions and Synthesis Processes:
In the chemical industry, (4-Benzyloxycarbonylaminophenyl)boronic acid, pinacol ester is used as a key component in various synthesis processes. Its role in facilitating the formation of carbon-carbon bonds makes it an essential tool for creating a wide range of organic compounds, contributing to the advancement of chemical research and development.
Used in the Development of New Drug Candidates:
(4-Benzyloxycarbonylaminophenyl)boronic acid, pinacol ester is utilized in the development of new drug candidates, where its ability to form carbon-carbon bonds is critical for the synthesis of novel and complex molecular structures with potential therapeutic applications.
Used in Fine Chemical Production:
In the production of fine chemicals, (4-Benzyloxycarbonylaminophenyl)boronic acid, pinacol ester is employed to synthesize high-quality specialty chemicals that require precise molecular structures. Its use in this industry is vital for the creation of high-value products with specific applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 363186-06-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,3,1,8 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 363186-06:
(8*3)+(7*6)+(6*3)+(5*1)+(4*8)+(3*6)+(2*0)+(1*6)=145
145 % 10 = 5
So 363186-06-5 is a valid CAS Registry Number.
InChI:InChI=1/C20H24BNO4/c1-19(2)20(3,4)26-21(25-19)16-10-12-17(13-11-16)22-18(23)24-14-15-8-6-5-7-9-15/h5-13H,14H2,1-4H3,(H,22,23)

363186-06-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzyl (4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate

1.2 Other means of identification

Product number -
Other names benzyl N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate

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:363186-06-5 SDS

363186-06-5Relevant academic research and scientific papers

FUROISOQUINOLINE DERIVATIVES, PROCESS FOR PRODUCING THE SAME AND USE THEREOF

-

, (2008/06/13)

A compound having a partial structure represented by Formula: or a salt thereof has an excellent phosphodiesterase (PDE) IV-inhibiting effect, and is useful as a prophylactic or therapeutic agent against inflammatory diseases, for example, bronchial asthma, chronic obstructive pulmonary disease (COPD), rheumatoid arthritis, autoimmune disease, diabetes and the like.

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