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4-(PENTAFLUOROSULFANYL)BENZOYL CHLORIDE, with the molecular formula C7H2ClF5S, is a benzoyl chloride derivative featuring a pentafluorosulfanyl (SF5) substituent on the benzene ring. 4-(PENTAFLUOROSULFANYL)BENZOYL CHLORIDE is recognized for its high reactivity and versatility, serving as a crucial intermediate in the synthesis of a variety of organic compounds. Its unique pentafluorosulfanyl group endows it with distinctive chemical properties, making it a valuable asset in introducing novel functionality into molecules.

197384-98-8

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197384-98-8 Usage

Uses

Used in Pharmaceutical Industry:
4-(PENTAFLUOROSULFANYL)BENZOYL CHLORIDE is used as a building block for the development of new drugs. Its reactivity and the unique properties of the pentafluorosulfanyl group allow for the creation of innovative pharmaceutical compounds with potential therapeutic benefits.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(PENTAFLUOROSULFANYL)BENZOYL CHLORIDE is utilized as a key intermediate in the synthesis of new pesticides. 4-(PENTAFLUOROSULFANYL)BENZOYL CHLORIDE's versatility in chemical reactions facilitates the design of effective and novel agrochemical products aimed at enhancing crop protection and yield.
Used in Organic Synthesis:
4-(PENTAFLUOROSULFANYL)BENZOYL CHLORIDE is employed as a reactive intermediate in a wide range of chemical reactions. Its high reactivity and the presence of the pentafluorosulfanyl group make it an important tool for organic synthesis, enabling the production of diverse organic compounds with various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 197384-98-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,3,8 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 197384-98:
(8*1)+(7*9)+(6*7)+(5*3)+(4*8)+(3*4)+(2*9)+(1*8)=198
198 % 10 = 8
So 197384-98-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H4ClF5OS/c8-7(14)5-1-3-6(4-2-5)15(9,10,11,12)13/h1-4H

197384-98-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H35498)  4-(Pentafluorothio)benzoyl chloride, 97%   

  • 197384-98-8

  • 1g

  • 740.0CNY

  • Detail
  • Alfa Aesar

  • (H35498)  4-(Pentafluorothio)benzoyl chloride, 97%   

  • 197384-98-8

  • 5g

  • 2470.0CNY

  • Detail

197384-98-8SDS

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-(pentafluoro-λ<sup>6</sup>-sulfanyl)benzoyl chloride

1.2 Other means of identification

Product number -
Other names 4-Pentafluorosulfanylbenzoylchloride

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:197384-98-8 SDS

197384-98-8Relevant academic research and scientific papers

Identification of orally-bioavailable antagonists of the TRPV4 ion-channel

Wei, Zhi-Liang,Nguyen, Margaret T.,O'Mahony, Donogh J.R.,Acevedo, Alejandra,Zipfel, Sheila,Zhang, Qingling,Liu, Luna,Dourado, Michelle,Chi, Candace,Yip, Victor,Defalco, Jeff,Gustafson, Amy,Emerling, Daniel E.,Kelly, Michael G.,Kincaid, John,Vincent, Fabien,Duncton, Matthew A.J.

, p. 4011 - 4015 (2015)

Abstract Antagonists of the TRPV4 receptor were identified using a focused screen, followed by a limited optimization program. The leading compounds obtained from this exercise, RN-1665 23 and RN-9893 26, showed moderate oral bioavailability when dosed to

METHOD FOR PRODUCING PENTAFLUOROSULFANYL BENZOIC ACID

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Paragraph 0073; 0074, (2014/10/28)

Provided is a simple, safe, and industrially practical method for producing a pentafluorosulfanylbenzoic acid. This method includes (A) a providing step of providing a trihalomethyl(pentafluorosulfanylbenzene) represented by general formula (1): where X i

AMIDOACETONITRILE COMPOUNDS AND PESTICIDAL COMPOSITION THEREOF

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Page/Page column 21, (2010/06/20)

The invention relates to compounds of the general formula (I) wherein the variable have the meanings as indicated in the claims, and optionally the enantiomers thereof. The active ingredients have advantageous pesticidal properties. They are especially su

ANTIPARASITIC AGENTS

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, (2008/12/07)

The present invention relates to compounds of the formula (I) or a tautomer or prodrug thereof, or a pharmaceutically acceptable salt of said compound, tautomer or prodrug, wherein: R1, R2, R3, R4 and R5 are each independently selected from H, halo, CN, CF3 and CONH2; compositions containing such compounds and the uses of such compounds as antiparasitic agents.

ANTIPARASITIC AGENTS

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Page/Page column 20, (2008/12/08)

The present invention relates to compounds of the formula (I) and pharmaceutically acceptable salts thereof, compositions containing such compounds and the uses of such compounds as antiparasitic agents.

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