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405-99-2

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405-99-2 Usage

Description

4-Fluorostyrene, also known as 4-fluorovinylbenzene, is an organic compound that serves as a crucial raw material and intermediate in various industries. It is a clear colorless to very slightly yellow liquid with significant chemical properties that make it valuable for a range of applications.

Uses

Used in Organic Synthesis:
4-Fluorostyrene is used as a key intermediate for the production of various organic compounds. Its unique chemical structure allows for the creation of a wide array of products, making it an essential component in this field.
Used in Pharmaceuticals:
In the pharmaceutical industry, 4-Fluorostyrene is utilized as a building block for the synthesis of various medicinal compounds. Its presence in the molecular structure can influence the properties and efficacy of the final drug, contributing to the development of novel therapeutic agents.
Used in Agrochemicals:
4-Fluorostyrene plays a vital role in the agrochemical sector as a starting material for the synthesis of various pesticides and other agricultural chemicals. Its incorporation into these products can enhance their effectiveness and selectivity, leading to improved crop protection and yield.
Used in Dyestuff:
In the dyestuff industry, 4-Fluorostyrene is employed as a precursor for the production of a variety of dyes and pigments. Its unique chemical properties enable the creation of vibrant and stable colorants that are used in various applications, such as textiles, plastics, and printing inks.

Check Digit Verification of cas no

The CAS Registry Mumber 405-99-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 405-99:
(5*4)+(4*0)+(3*5)+(2*9)+(1*9)=62
62 % 10 = 2
So 405-99-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H7F/c1-2-7-3-5-8(9)6-4-7/h2-6H,1H2

405-99-2 Well-known Company Product Price

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  • Aldrich

  • (155799)  4-Fluorostyrene  99%, contains tert-butylcatechol as inhibitor

  • 405-99-2

  • 155799-1G

  • 401.31CNY

  • Detail
  • Aldrich

  • (155799)  4-Fluorostyrene  99%, contains tert-butylcatechol as inhibitor

  • 405-99-2

  • 155799-10G

  • 1,682.46CNY

  • Detail

405-99-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Fluorostyrene

1.2 Other means of identification

Product number -
Other names 1-Fluoro-4-vinylbenzene

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:405-99-2 SDS

405-99-2Relevant articles and documents

Mild and efficient desulfurization of thiiranes with MoCl5/Zn system

Lee, Yeong Jin,Shin, Jeong Won,Yoo, Byung Woo

, (2021/11/10)

Desulfurization of a variety of thiiranes to alkenes occurs chemoselectively in high yields upon treatment with MoCl5/Zn system under mild conditions. The new methodology demonstrates high functional group tolerance toward chloro, bromo, fluoro, methoxy, ester, ether and keto groups.

Boronic Acid Pairs for Sequential Bioconjugation

Ball, Zachary T.,Ding, Yuxuan,Miller, Mary K.,Swierczynski, Michael J.

supporting information, p. 5334 - 5338 (2021/07/26)

Boronic acids can play diverse roles when applied in biological environments, and employing boronic acid structures in tandem could provide new tools for multifunctional probes. This Letter describes a pair of boronic acid functional groups, 2-nitro-arylboronic acid (NAB) and (E)-alkenylboronic acid (EAB), that enable sequential cross-coupling through stepwise nickel- and copper-catalyzed processes. The selective coupling of NAB groups enables the preparation of stapled peptides, protein-protein conjugates, and other bioconjugates.

Controlling the Lewis Acidity and Polymerizing Effectively Prevent Frustrated Lewis Pairs from Deactivation in the Hydrogenation of Terminal Alkynes

Geng, Jiao,Hu, Xingbang,Liu, Qiang,Wu, Youting,Yang, Liu,Yao, Chenfei

, p. 3685 - 3690 (2021/05/31)

Two strategies were reported to prevent the deactivation of Frustrated Lewis pairs (FLPs) in the hydrogenation of terminal alkynes: reducing the Lewis acidity and polymerizing the Lewis acid. A polymeric Lewis acid (P-BPh3) with high stability was designed and synthesized. Excellent conversion (up to 99%) and selectivity can be achieved in the hydrogenation of terminal alkynes catalyzed by P-BPh3. This catalytic system works quite well for different substrates. In addition, the P-BPh3 can be easily recycled.

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