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3-(4-MORPHOLINOMETHYL)-PHENYLBORONIC ACID PINACOL ESTER HYDROCHLORIDE is a boronic acid pinacol ester derivative featuring a morpholine group. This hydrochloride salt form of the compound is known for its enhanced solubility in water and other polar solvents, making it a versatile molecule in the realms of organic synthesis and medicinal chemistry. Its unique structure and properties have positioned it as a promising candidate for inhibiting enzyme activity and as a building block in the synthesis of biologically active molecules, thus holding significant value for the development of new pharmaceuticals and other organic compounds.

1073371-76-2

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1073371-76-2 Usage

Uses

Used in Organic Synthesis:
3-(4-MORPHOLINOMETHYL)-PHENYLBORONIC ACID PINACOL ESTER HYDROCHLORIDE is used as a synthetic intermediate for the creation of various organic compounds. Its reactivity and functional groups allow for the formation of new chemical bonds and the synthesis of complex molecules that can be utilized in a wide range of applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-(4-MORPHOLINOMETHYL)-PHENYLBORONIC ACID PINACOL ESTER HYDROCHLORIDE is used as a potential inhibitor of enzyme activity. Its ability to interact with enzymes can lead to the development of new drugs that target specific biological pathways, offering therapeutic benefits in treating various diseases.
Used in Pharmaceutical Development:
3-(4-MORPHOLINOMETHYL)-PHENYLBORONIC ACID PINACOL ESTER HYDROCHLORIDE is used as a building block in the synthesis of biologically active molecules for pharmaceutical development. Its unique structure contributes to the design of novel compounds with potential therapeutic effects, advancing the discovery of new drugs and treatments.
Used in Chemical Research:
In the research industry, 3-(4-MORPHOLINOMETHYL)-PHENYLBORONIC ACID PINACOL ESTER HYDROCHLORIDE is used as a research tool to study the properties and reactions of boronic acid pinacol esters. Understanding its behavior in chemical reactions can provide insights into the development of new synthetic methods and the creation of new chemical entities.

Check Digit Verification of cas no

The CAS Registry Mumber 1073371-76-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,3,7 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1073371-76:
(9*1)+(8*0)+(7*7)+(6*3)+(5*3)+(4*7)+(3*1)+(2*7)+(1*6)=142
142 % 10 = 2
So 1073371-76-2 is a valid CAS Registry Number.

1073371-76-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-Morpholinomethyl)phenylboronic acidpinacol ester,HCl

1.2 Other means of identification

Product number -
Other names 3-Thiophenecarbonitrile,4-[[4-(methylthio)-2-nitrophenyl]amino]

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:1073371-76-2 SDS

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