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247129-85-7

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247129-85-7 Usage

Uses

Reactant for:Sulfinylation reactionsCyclization reactionsAnnulation reactions

Check Digit Verification of cas no

The CAS Registry Mumber 247129-85-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,7,1,2 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 247129-85:
(8*2)+(7*4)+(6*7)+(5*1)+(4*2)+(3*9)+(2*8)+(1*5)=147
147 % 10 = 7
So 247129-85-7 is a valid CAS Registry Number.

247129-85-7 Well-known Company Product Price

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  • Aldrich

  • (706345)  (2-Bromoethyl)diphenylsulfoniumtrifluoromethanesulfonate  97%

  • 247129-85-7

  • 706345-1G

  • 630.63CNY

  • Detail
  • Aldrich

  • (706345)  (2-Bromoethyl)diphenylsulfoniumtrifluoromethanesulfonate  97%

  • 247129-85-7

  • 706345-5G

  • 2,142.27CNY

  • Detail

247129-85-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromoethyl(diphenyl)sulfanium,trifluoromethanesulfonate

1.2 Other means of identification

Product number -
Other names (2-Bromoethyl)diphenylsulfonium Trifluoromethanesulfonate

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:247129-85-7 SDS

247129-85-7Relevant articles and documents

Vinyl Thianthrenium Tetrafluoroborate: A Practical and Versatile Vinylating Reagent Made from Ethylene

Juliá, Fabio,Paulus, Fritz,Ritter, Tobias,Yan, Jiyao

supporting information, p. 12992 - 12998 (2021/09/03)

The use of vinyl electrophiles in synthesis has been hampered by the lack of access to a suitable reagent that is practical and of appropriate reactivity. In this work we introduce a vinyl thianthrenium salt as an effective vinylating reagent. The bench-stable, crystalline reagent can be readily prepared from ethylene gas at atmospheric pressure in one step and is broadly useful in the annulation chemistry of (hetero)cycles, N-vinylation of heterocyclic compounds, and palladium-catalyzed cross-coupling reactions. The structural features of the thianthrene core enable a distinct synthesis and reactivity profile, unprecedented for other vinyl sulfonium derivatives.

Annulation of β-naphthols and 4-hydroxycoumarins with vinylsulfonium salts: Synthesis of dihydrofuran derivatives

Chen, Zi-Cong,Tong, Lang,Du, Zhi-Bo,Mao, Zhi-Feng,Zhang, Xue-Jing,Zou, Yong,Yan, Ming

supporting information, p. 2634 - 2638 (2018/04/26)

A new synthetic approach to dihydrofuran derivatives via the annulation reaction of β-naphthols and 4-hydroxycoumarins with vinylsulfonium salts has been developed. A variety of dihydrofuran derivatives were prepared in moderate to good yields under mild conditions. The products could be readily transformed to the corresponding furans via the dehydrogenation with DDQ.

A convenient cyclopropanation process of oxindoles via bromoethylsulfonium salt

Qin, Hui,Miao, Yuanyuan,Zhang, Ke,Xu, Jian,Sun, Haopeng,Liu, Wenyuan,Feng, Feng,Qu, Wei

, p. 6809 - 6814 (2018/10/20)

A practical convenient conversion of oxindoles into the corresponding spirocyclopropyl oxindoles is achieved efficiently using bromoethylsulfonium salt, which is easily prepared on a large scale and is stable crystalline. This reaction of bromoethylsulfonium salt with different substituted unprotected oxindoles proceeded under mild condition and provided moderate yields.

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