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27081-10-3

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27081-10-3 Usage

Description

Tropylium Tetrafluoroborate, with the chemical formula C7H7BF4 and CAS# 27081-10-3, is an off-white to beige powder. It is a versatile reagent and reactant used in various chemical reactions and applications due to its unique properties.

Uses

1. Used in Chemical Synthesis:
Tropylium Tetrafluoroborate is used as a reactant or reagent for several chemical reactions, including:
a. Retro-Buchner reactions for the synthesis of arylcyclopropanes.
b. Desymmetrization for access to homocalystegine analogs or aminocycloheptitols.
c. α-Cyanation of imines.
d. Stereoselective α-alkylation of aldehydes with stable carbocations.
e. Oxidative C-H activation of aliphatic aldehydes.
f. Electrochemical Redox transformations.
2. Used in Electrochemical Applications:
Tropylium Tetrafluoroborate is used as an electrolytic solution for electrochemical devices, providing a medium for ionic conduction and facilitating various electrochemical processes.
3. Used in Protective Coatings:
Tropylium Tetrafluoroborate is used as a component in protective coatings for selenium electrophotographic plates, enhancing their durability and performance.

Check Digit Verification of cas no

The CAS Registry Mumber 27081-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,8 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27081-10:
(7*2)+(6*7)+(5*0)+(4*8)+(3*1)+(2*1)+(1*0)=93
93 % 10 = 3
So 27081-10-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H7.BF4/c1-2-4-6-7-5-3-1;2-1(3,4)5/h1-5H,6H2;/q+1;-1

27081-10-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Alfa Aesar

  • (A14045)  Tropylium tetrafluoroborate, 97%   

  • 27081-10-3

  • 5g

  • 801.0CNY

  • Detail
  • Alfa Aesar

  • (A14045)  Tropylium tetrafluoroborate, 97%   

  • 27081-10-3

  • 25g

  • 2182.0CNY

  • Detail
  • Alfa Aesar

  • (A14045)  Tropylium tetrafluoroborate, 97%   

  • 27081-10-3

  • 100g

  • 8648.0CNY

  • Detail
  • Aldrich

  • (164623)  Tropyliumtetrafluoroborate  97%

  • 27081-10-3

  • 164623-10G

  • 7,119.45CNY

  • Detail
  • Aldrich

  • (164623)  Tropyliumtetrafluoroborate  97%

  • 27081-10-3

  • 164623-25G

  • 12,671.10CNY

  • Detail

27081-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohepta-1,3,5-triene,tetrafluoroborate

1.2 Other means of identification

Product number -
Other names TropyliuM Tetrafluoroborate

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:27081-10-3 SDS

27081-10-3Relevant articles and documents

Synthesis of 1,3-Dithiol-2-yl and 1,3-Benzodithiol-2-yl Azides and Their Reaction with Trityl Salt

Nakayama, Juzo,Fujiwara, Kazuo,Hoshino, Masamatsu

, p. 2024 - 2025 (1980)

-

-

Dauben,Jr. et al.

, p. 1442,1444 (1960)

-

Synthesis and Isolation of Polytrityl Cations by Utilizing Hexaphenylbenzene and Tetraphenylmethane Scaffolds

Rathore, Rajendra,Burns, Carrie L.,Guzei, Ilia A.

, p. 1524 - 1530 (2007/10/03)

The successful isolation of stable (and soluble) hexa- and tetratrityl cations based on hexaphenyl-benzene and tetraphenylmethane scaffold has been accomplished by using readily available starting materials. These robust polytrityl cations can be isolated in crystalline form and stored indefinitely at 0 °C. Their structures have been established by 1H/ 13C NMR spectroscopy and by UV-vis spectroscopy. The structures of these polytrityl cations were further confirmed by quantitative transformations to the reduced (poly)triphenylmethyl derivatives by hydride transfer from triethylsilane, cycloheptatriene, or a borane-dimethyl sulfide complex.

Cyclisation reactions of 2-substituted biphenyl-2'-yldiazonium salts leading to O-alkyldibenzofuranium and S-alkyldibenzothiophenium salts: Modified Meerwein reagents

Downie,Heaney,Kemp,King,Wosley

, p. 4005 - 4016 (2007/10/02)

The preparation of 2-amino-2'-methoxybiphenyl and 2-amino-2'-thiomethoxybiphenyl and analogues and their transformation into diazonium salts and hence into dibenzofuranium and dibenzothiophenium salts is described together with their use as alkylating agents.

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