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2,3,4,5,6-PENTAFLUOROPHENYL 4-BROMOBENZENESULFONATE is a chemical compound derived from benzene, featuring a pentafluorophenyl group attached to a 4-bromobenzenesulfonate group. It is recognized for its high reactivity and is utilized in various applications across different industries, including pharmaceuticals, agrochemicals, and the synthesis of complex organic compounds.

848649-38-7

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848649-38-7 Usage

Uses

Used in Organic Synthesis:
2,3,4,5,6-PENTAFLUOROPHENYL 4-BROMOBENZENESULFONATE is used as a reagent in organic synthesis for its high reactivity, facilitating the formation of new chemical bonds and structures.
Used in Chemical Research:
In the field of chemical research, 2,3,4,5,6-PENTAFLUOROPHENYL 4-BROMOBENZENESULFONATE serves as an intermediate, contributing to the development of new methodologies and understanding of chemical reactions.
Used in Pharmaceutical Industry:
2,3,4,5,6-PENTAFLUOROPHENYL 4-BROMOBENZENESULFONATE is used as a building block in the production of pharmaceuticals, aiding in the creation of new drugs and improving the efficacy of existing ones.
Used in Agrochemical Industry:
2,3,4,5,6-PENTAFLUOROPHENYL 4-BROMOBENZENESULFONATE is also utilized in the agrochemical sector, where it is employed in the synthesis of pesticides and other agricultural chemicals to enhance crop protection and yield.
Used in Material Development:
2,3,4,5,6-PENTAFLUOROPHENYL 4-BROMOBENZENESULFONATE is used in the development of new materials, contributing to the advancement of various material sciences and the creation of innovative products with unique properties.
Used in Synthesis of Complex Organic Compounds:
As a key component in the synthesis of more complex organic compounds, 2,3,4,5,6-PENTAFLUOROPHENYL 4-BROMOBENZENESULFONATE is instrumental in expanding the scope of organic chemistry and enabling the discovery of novel molecules with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 848649-38-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,6,4 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 848649-38:
(8*8)+(7*4)+(6*8)+(5*6)+(4*4)+(3*9)+(2*3)+(1*8)=227
227 % 10 = 7
So 848649-38-7 is a valid CAS Registry Number.

848649-38-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,3,4,5,6-pentafluorophenyl) 4-bromobenzenesulfonate

1.2 Other means of identification

Product number -
Other names perfluorophenyl 4-bromobenzenesulfonate

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:848649-38-7 SDS

848649-38-7Relevant academic research and scientific papers

Pentafluorophenyl sulfonate ester as a protecting group for the preparation of biaryl- and heterobiaryl sulfonate esters

Avitabile, Barbara G.,Smith, Clive A.,Judd, Duncan B.

, p. 843 - 846 (2005)

(Chemical Equation Presented) The use of the pentafluorophenyl (PFP) group as a sulfonic acid protecting group has allowed the synthesis of new biaryl- and heterobiaryl-PFP-sulfonate esters by use of the Suzuki-Miyaura reaction. The successful employment

One-Pot Synthesis of Pentafluorophenyl Sulfonic Esters via Copper-Catalyzed Reaction of Aryl Diazonium Salts, DABSO, and Pentafluorophenol

Idris, Muhammad Aliyu,Lee, Sunwoo

supporting information, p. 4516 - 4520 (2021/05/26)

Pentafluorophenyl (PFP) sulfonic esters were synthesized via a copper-catalyzed one-pot multicomponent reaction of aryl diazonium tetrafluoroborate, DABSO (DABCO·(SO2)2), and pentafluorophenol. The reaction system provided the desired pentafluorophenyl sulfonic esters in good yields and exhibited excellent functional group tolerance. In addition, the generated PFP sulfonic esters were successfully applied in Sonogashira, Suzuki, Chan-Evans-Lam, and decarboxylative coupling reactions.

Copper-Catalyzed Synthesis of Activated Sulfonate Esters from Boronic Acids, DABSO, and Pentafluorophenol

Vedovato, Vincent,Talbot, Eric P. A.,Willis, Michael C.

supporting information, p. 5493 - 5496 (2018/09/12)

The synthesis of pentafluorophenyl (PFP) sulfonate esters based on the Pd-catalyzed sulfination of aryl and heteroaryl boronic acids is reported. The sulfinate intermediates are converted in situ to the corresponding sulfonate esters using a copper-catalyzed oxidative process, providing a broad range of PFP esters in good yields.

PYRIDINE COMPOUNDS AND AZA ANALOGUES THEREOF AS TYK2 INHIBITORS

-

Page/Page column 52, (2012/05/31)

The present invention relates to compounds of formula (I), wherein R1 to R3, X1, X2 have the meaning as cited in the description and the claims. Said compounds are useful as TYK2 inhibitors for the treatment or prophylaxis of immunological, inflammatory, autoimmune, allergic disorders, and immunologically-mediated diseases. The invention also relates to pharmaceutical compositions including said compounds as well as their use as medicaments.

O-HYDROXY- AND O-AMINO BENZAMIDE DERIVATIVES AS IKK2 INHIBITORS

-

Page/Page column 43, (2010/11/26)

A compound of Formula (I).

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