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7182-86-7

7182-86-7

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7182-86-7 Usage

Uses

Tetrabutylammonium p-toluenesulfonate (TBAOTs) can be used as: A phase transfer catalyst (PTC) in SN2 fluorinations.An electrolyte in the preparation of conducting polymer polypyrrole (PPy) by electrochemical polymerization technique. A reagent to synthesize 1-alkynyl sulfonates from 1-alkynyl-bromanes by Michael-carbene rearrangement reaction.

Check Digit Verification of cas no

The CAS Registry Mumber 7182-86-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,8 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7182-86:
(6*7)+(5*1)+(4*8)+(3*2)+(2*8)+(1*6)=107
107 % 10 = 7
So 7182-86-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H36N.C7H8O3S/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;1-6-2-4-7(5-3-6)11(8,9)10/h5-16H2,1-4H3;2-5H,1H3,(H,8,9,10)/q+1;/p-1

7182-86-7 Well-known Company Product Price

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  • Aldrich

  • (358681)  Tetrabutylammoniump-toluenesulfonate  99%

  • 7182-86-7

  • 358681-2G

  • 469.17CNY

  • Detail

  • Aldrich

  • (358681)  Tetrabutylammoniump-toluenesulfonate  99%

  • 7182-86-7

  • 358681-10G

  • 1,291.68CNY

  • Detail

7182-86-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylbenzenesulfonate,tetrabutylazanium

1.2 Other means of identification

Product number -
Other names tetrabutylammonium tosylate

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:7182-86-7 SDS

7182-86-7Relevant articles and documents

Visible-Light-Induced Nickel-Catalyzed Cross-Coupling with Alkylzirconocenes from Unactivated Alkenes

Bai, Songlin,Gao, Yadong,Jiang, Chao,Liu, Xiaolei,Qi, Xiangbing,Wang, Jing,Wu, Qingcui,Yang, Chao

supporting information, p. 675 - 688 (2020/03/11)

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Efficient method for varying the anions in quaternary onium halides

Jeon, Jong Yeob,Varghese, Jobi Kodiyan,Park, Ji Hae,Lee, Suck-Hyun,Lee, Bun Yeoul

experimental part, p. 3566 - 3569 (2012/08/14)

Quaternary onium salts of halides can be efficiently converted into the corresponding quaternary onium salts of various anions [NO3 -, BF4-, PF6-, CF 3SO3-, CH3SO3 -, ClO4-, p-CH3C6H 4SO3-, CF3CO2 -, 2,4-(NO2)2C6H3O -] by treating the onium halide with trimethyl phosphate under neat condition in the presence of an equivalent amount of conjugate acid of the desired anion.

Substratspezifische Katalyse durch Ionenpaare

Smith, Paul J.,Kim, Eun-il,Wilcox, Craig S.

, p. 1728 - 1730 (2007/10/02)

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