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45762-41-2

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45762-41-2 Usage

Description

4-BROMO-2-ETHYLANILINE is an organic compound that serves as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. It is characterized by the presence of a bromo and an ethyl group attached to the aniline moiety, which contributes to its reactivity and potential applications in chemical synthesis.

Uses

Used in Pharmaceutical Industry:
4-BROMO-2-ETHYLANILINE is used as a synthetic intermediate for the preparation of heteroaryl (arylamino)quinazoline derivatives, which have demonstrated in vitro antitumor activity. This makes it a valuable compound in the development of new and effective cancer treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 45762-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,7,6 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 45762-41:
(7*4)+(6*5)+(5*7)+(4*6)+(3*2)+(2*4)+(1*1)=132
132 % 10 = 2
So 45762-41-2 is a valid CAS Registry Number.

45762-41-2 Well-known Company Product Price

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  • Alfa Aesar

  • (L12725)  4-Bromo-2-ethylaniline, 97%   

  • 45762-41-2

  • 5g

  • 498.0CNY

  • Detail
  • Alfa Aesar

  • (L12725)  4-Bromo-2-ethylaniline, 97%   

  • 45762-41-2

  • 25g

  • 1714.0CNY

  • Detail

45762-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Bromo-2-ethylaniline

1.2 Other means of identification

Product number -
Other names 4-BROMO-2-ETHYLANILINE

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:45762-41-2 SDS

45762-41-2Relevant articles and documents

Donor-substituted distyrylpyrazines: Influence of steric congestion on UV-Vis absorption and fluorescence

Wink, Christoph,Detert, Heiner

supporting information, p. 144 - 150 (2013/03/13)

Di(p-aminostyryl)pyrazines with voluminous substituents on the nitrogen and in the adjacent positions were prepared via twofold aldol condensation. Absorption and emission spectra are influenced by increasing steric hindrance because the orbital overlap between nitrogen and π-system is modulated by voluminous groups. Strong solvatochromism of the fluorescence and huge Stokes shifts result from amplified donor-acceptor interaction in the excited state. Protonation occurs at the terminal amino groups first, followed by protonation of the central pyrazine. With increasing strength of acid, absorption and emission spectra are first shifted to the blue followed by a redshift. Copyright

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