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4-Chloro-2-fluorobenzyl amine, with the molecular formula C7H6ClFN and IUPAC name 4-Chloro-2-fluorobenzenemethanamine, is a chemical compound belonging to the class of organic compounds known as benzene and its substituted derivatives. It is an aromatic compound with a monocyclic ring system made of benzene, featuring chlorine and fluorine substituents on the benzene ring. 4-CHLORO-2-FLUOROBENZYL AMINE's reactivity and toxicity are determined by its precise molecular structure, and it has applications in various areas of chemistry, particularly in the synthesis of more complex chemical compounds.

72235-57-5

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72235-57-5 Usage

Uses

Used in Chemical Synthesis:
4-Chloro-2-fluorobenzyl amine is used as a chemical intermediate for the synthesis of more complex chemical compounds. Its unique molecular structure, with chlorine and fluorine substituents, allows for versatile reactivity in chemical reactions, making it a valuable component in the creation of advanced molecules for various applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Chloro-2-fluorobenzyl amine is used as a building block for the development of new drugs. Its specific molecular structure can be utilized to create novel compounds with potential therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Material Science:
4-Chloro-2-fluorobenzyl amine is employed in material science as a component in the design and synthesis of new materials with unique properties. Its incorporation into polymers or other materials can lead to the development of innovative products with enhanced characteristics, such as improved stability or reactivity.
Used in Research and Development:
In research and development settings, 4-Chloro-2-fluorobenzyl amine is used as a reagent or starting material for exploring new chemical reactions and pathways. Its presence in various chemical processes can provide insights into the behavior of similar compounds and contribute to the understanding of chemical mechanisms.

Check Digit Verification of cas no

The CAS Registry Mumber 72235-57-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,2,3 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 72235-57:
(7*7)+(6*2)+(5*2)+(4*3)+(3*5)+(2*5)+(1*7)=115
115 % 10 = 5
So 72235-57-5 is a valid CAS Registry Number.

72235-57-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H26352)  4-Chloro-2-fluorobenzylamine, 97%   

  • 72235-57-5

  • 1g

  • 1243.0CNY

  • Detail
  • Alfa Aesar

  • (H26352)  4-Chloro-2-fluorobenzylamine, 97%   

  • 72235-57-5

  • 5g

  • 3820.0CNY

  • Detail

72235-57-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-chloro-2-fluorophenyl)methanamine

1.2 Other means of identification

Product number -
Other names 4-CHLORO-2-FLUOROBENZYL AMINE

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:72235-57-5 SDS

72235-57-5Relevant academic research and scientific papers

Novel 1,4-benzodiazepine-2,5-diones as Hdm2 antagonists with improved cellular activity

Leonard, Kristi,Marugan, Juan Jose,Raboisson, Pierre,Calvo, Raul,Gushue, Joan M.,Koblish, Holly K.,Lattanze, Jennifer,Zhao, Shuyuan,Cummings, Maxwell D.,Player, Mark R.,Maroney, Anna C.,Lu, Tianbao

, p. 3463 - 3468 (2007/10/03)

The disruption of the p53-Hdm2 protein-protein interaction induces cell growth arrest and apoptosis. We have identified the 1,4-benzodiazepine-2,5-dione scaffold as a suitable template for inhibiting this interaction by binding to the Hdm2 protein. Several compounds have been made with improved potency, solubility, and cell-based activities.

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