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4-Fluorophenethyl isocyanate 97 is a chemical compound that serves as a versatile intermediate in the synthesis of complex organic molecules, particularly in the production of pharmaceuticals, agrochemicals, and organic materials. As a type of isocyanate, it exhibits high reactivity, which is instrumental in the creation of polyurethane foams, elastomers, adhesives, and coatings. The presence of a fluorine atom and a phenethyl group in its structure enhances its utility in various chemical reactions, although it requires careful handling due to its potential health hazards and reactivity.

65535-53-7

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65535-53-7 Usage

Uses

Used in Pharmaceutical Industry:
4-Fluorophenethyl isocyanate 97 is used as a key intermediate in the synthesis of pharmaceutical compounds for its ability to contribute to the development of novel drugs with specific therapeutic properties. Its unique structure allows for the creation of molecules with tailored pharmacological activities.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Fluorophenethyl isocyanate 97 is utilized as a reactive building block in the production of pesticides and other crop protection agents, enhancing their effectiveness and selectivity in agricultural applications.
Used in Organic Material Production:
4-Fluorophenethyl isocyanate 97 is employed as a crucial component in the synthesis of advanced organic materials, such as specialty polymers and high-performance materials, due to its capacity to impart specific characteristics to these materials, like improved thermal stability or chemical resistance.
Used in Polyurethane and Elastomer Production:
As a highly reactive isocyanate, 4-Fluorophenethyl isocyanate 97 is used in the manufacturing process of polyurethane foams and elastomers, contributing to their formation and determining their final properties, such as flexibility, durability, and resilience.
Used in Adhesive and Coating Formulation:
4-Fluorophenethyl isocyanate 97 is incorporated into the formulation of adhesives and coatings to enhance their bonding strength, durability, and resistance to environmental factors, thanks to its reactive nature and ability to form strong cross-linked networks.

Check Digit Verification of cas no

The CAS Registry Mumber 65535-53-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,3 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65535-53:
(7*6)+(6*5)+(5*5)+(4*3)+(3*5)+(2*5)+(1*3)=137
137 % 10 = 7
So 65535-53-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H8FNO/c10-9-3-1-8(2-4-9)5-6-11-7-12/h1-4H,5-6H2

65535-53-7 Well-known Company Product Price

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  • Aldrich

  • (571857)  4-Fluorophenethylisocyanate  97%

  • 65535-53-7

  • 571857-1G

  • 731.25CNY

  • Detail
  • Aldrich

  • (571857)  4-Fluorophenethylisocyanate  97%

  • 65535-53-7

  • 571857-5G

  • 2,666.43CNY

  • Detail

65535-53-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-fluoro-4-(2-isocyanatoethyl)benzene

1.2 Other means of identification

Product number -
Other names 4-fluorophenethyl isocyanate

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:65535-53-7 SDS

65535-53-7Relevant academic research and scientific papers

Synthesis and evaluation of novel compounds as potent dipeptidyl peptidase IV inhibitors

Wang, Liutang,Zhang, Bin,Ji, Jianxin,Li, Bogang,Yan, Jufang,Zhang, Weiyu,Wu, Yong,Wang, Xuechao,Hou, Hui

experimental part, p. 52 - 57 (2010/03/24)

A series of new 2-cyanopyrrolidine derivatives with constrained imidazolidin ring were synthesized, Their structures were confirmed by 1H NMR spectroscopy and/or mass spectrometry, and their activities were evaluated in vitro. They were proven to possess submicromolar inhibitory activities against dipeptidyl peptidase IV.

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