Welcome to LookChem.com Sign In|Join Free
  • or
Benzenepropanoic acid, .alpha.,.beta.-dibromo-4-fluoro-, ethyl ester is a chemical compound characterized by its molecular formula C11H10Br2FO2. It features a benzene ring with bromine and fluorine atoms attached, making it a versatile intermediate in organic synthesis and pharmaceutical research. Benzenepropanoic acid, .alpha.,.beta.-dibroMo-4-fluoro-, ethyl e is known for its potential in various reactions and applications, particularly in the production of pharmaceutical drugs, agrochemicals, and other fine chemicals. Its unique structure also lends itself to the development of new materials and compounds with specific properties. However, it requires careful handling and storage due to its potential hazards.

42122-47-4

Post Buying Request

42122-47-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

42122-47-4 Usage

Uses

Used in Pharmaceutical Research and Development:
Benzenepropanoic acid, .alpha.,.beta.-dibromo-4-fluoro-, ethyl ester is utilized as an intermediate in the synthesis of pharmaceutical drugs. Its unique structure allows for the development of new compounds with specific therapeutic properties, contributing to the advancement of medicine.
Used in Agrochemical Production:
This chemical compound is also employed in the production of agrochemicals, where its reactive bromine and fluorine atoms can be used to create new compounds with targeted effects on pests or crops, enhancing agricultural productivity and crop protection.
Used in the Synthesis of Fine Chemicals:
Benzenepropanoic acid, .alpha.,.beta.-dibromo-4-fluoro-, ethyl ester is used in the synthesis of fine chemicals, which are high-purity chemicals used in various industries, including fragrances, flavors, and specialty chemicals. Its unique structure allows for the creation of new compounds with specific properties, expanding the range of applications in these industries.
Used in the Development of New Materials:
Benzenepropanoic acid, .alpha.,.beta.-dibroMo-4-fluoro-, ethyl e's potential applications extend to the development of new materials with specific properties. Its unique structure and reactivity make it a valuable component in the creation of innovative materials for various industries, such as electronics, plastics, and coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 42122-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,1,2 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 42122-47:
(7*4)+(6*2)+(5*1)+(4*2)+(3*2)+(2*4)+(1*7)=74
74 % 10 = 4
So 42122-47-4 is a valid CAS Registry Number.

42122-47-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dibromo-3-(4-fluoro-phenyl)-propionic acid ethyl ester

1.2 Other means of identification

Product number -
Other names ETHYL 2,3-DIBROMO-3-(4-FLUOROPHENYL)PROPANOATE

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:42122-47-4 SDS

42122-47-4Relevant academic research and scientific papers

SUBSTITUTED 1-PROPIOLYLPIPERAZINES HAVING AN AFFINITY FOR THE MGLUR5 RECEPTOR IN ORDER TO TREAT PAINFUL CONDITIONS

-

Page/Page column 98, (2010/02/15)

The invention relates to substituted 1-propiolylpiperazines according to formula (I), to a method for the production thereof, medicaments containing said compounds and to the use thereof in the production of medicaments. In formula (I), X represents N or C-R2 and n corresponds to a value between 0-8.

Transmission of substituent effects through extended systems-III. p-Substituted ethyl trans cinnamates and phenylpropiolates

Butt, G.,Topsom, R. D.

, p. 649 - 654 (2007/10/02)

Infrared data and 13C chemical shifts are reported for a series of ethyl p-substituted trans-cinnamates and ethyl phenylpropiolates.The i.r. values include intensities for the benzene, ethylene and carbonyl vibrations which allow an estimation of resonance effects.The relative importance of the various mechanisms of transmission of substituent effects are discussed and compared to those previously reported for p-substituted trans cinnamonitriles.It is shown that the carbon-carbon triple bond is less efficient in transmitting substituent effects than carbon-carbon double bonds.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 42122-47-4