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874291-00-6

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874291-00-6 Usage

Description

4-[(Ethylcarbamoyl)amino]benzenboronic acid, pinacol ester 98% and 4-(3-ethylureido)benzenboronic acid, pinacol ester are both organic compounds widely used in chemical research and pharmaceutical synthesis. They serve as reagents and intermediates in the production of various pharmaceuticals, agrochemicals, and advanced materials. These chemicals are known for their potential in drug discovery and development, and their high purity form (98%) makes them suitable for use in advanced research and development projects.

Uses

Used in Pharmaceutical Synthesis:
4-[(Ethylcarbamoyl)amino]benzenboronic acid, pinacol ester 98% and 4-(3-ethylureido)benzenboronic acid, pinacol ester are used as reagents and intermediates in the synthesis of various pharmaceuticals. They contribute to the development of new drugs and the improvement of existing ones.
Used in Agrochemical Production:
In the agrochemical industry, these compounds are used as reagents and intermediates in the production of various agrochemicals. They help in the development of new agrochemicals and the enhancement of existing ones, contributing to improved crop protection and yield.
Used in Advanced Materials Development:
4-[(Ethylcarbamoyl)amino]benzenboronic acid, pinacol ester 98% and 4-(3-ethylureido)benzenboronic acid, pinacol ester are utilized in the development of advanced materials, such as sensors, catalysts, and other specialty materials. Their unique properties make them valuable in creating innovative materials with specific functions and applications.
Used in Drug Discovery and Development:
These organic compounds are employed in drug discovery and development processes, where they are used to synthesize bioactive molecules with potential therapeutic effects. Their high purity (98%) ensures the quality and reliability of the synthesized compounds, facilitating the advancement of new drug candidates.

Check Digit Verification of cas no

The CAS Registry Mumber 874291-00-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,2,9 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 874291-00:
(8*8)+(7*7)+(6*4)+(5*2)+(4*9)+(3*1)+(2*0)+(1*0)=186
186 % 10 = 6
So 874291-00-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H23BN2O3/c1-6-17-13(19)18-12-9-7-11(8-10-12)16-20-14(2,3)15(4,5)21-16/h7-10H,6H2,1-5H3,(H2,17,18,19)

874291-00-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H52953)  4-(3-Ethylureido)benzeneboronic acid pinacol ester, 98%   

  • 874291-00-6

  • 250mg

  • 882.0CNY

  • Detail
  • Alfa Aesar

  • (H52953)  4-(3-Ethylureido)benzeneboronic acid pinacol ester, 98%   

  • 874291-00-6

  • 1g

  • 2822.0CNY

  • Detail

874291-00-6SDS

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 1-Ethyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea

1.2 Other means of identification

Product number -
Other names 1-ethyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea

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:874291-00-6 SDS

874291-00-6Relevant articles and documents

As the PI3K/mTOR inhibitor tricyclic compound, its preparation and use

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Paragraph 0168; 0170, (2017/08/25)

The invention discloses a tricyclic compound as a PI3K/mTOR inhibitor. The tricyclic compound is a compound with the general formula (I) in the specification, wherein Ar is selected from aryl or heteroaryl; X, Y and Z are independently selected from O, CR2R3 and NR4 respectively; Q is selected from O, CR2R3 and NR4 or does not exists; R1 represents C1-C6 alkyl; n is selected from integers from 0 to 4; when n is more than or equal to 2, two R1 and a morpholine cycle can be combined into a combined cycle, a bridge cycle or a spiral cycle; R2 and R3 are selected from hydrogen and C1-C6 alkyl; R4 is selected from hydrogen, C1-C6 alkyl, C3-C7 cycloalkyl, heterocyclic radical, acyl and sulfonyl. The invention further discloses a perpetration method of the compound with the general formula (I) as well as a pharmaceutical composition and application of the compound with the general formula (I).

Having a spiro ring substituent of aryl morpholine compound, its preparation and use

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, (2017/08/02)

The invention discloses arylmorpholine compounds with spiro substituents. The arylmorpholine compounds are compounds having the following general formula (I), wherein X is N or CH; R1 is hydrogen, hydroxyl, alkoxy, halogen, amino, amido, acylamino, sulfam

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