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2919-23-5

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2919-23-5 Usage

Chemical Properties

CLEAR COLOURLESS LIQUID

Uses

Has synthetic applications of gold-catalyzed ring expansions. Development of novel type of transition metal-catalyzed cascade reactions utilizing small ring systems and the applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2919-23-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2919-23:
(6*2)+(5*9)+(4*1)+(3*9)+(2*2)+(1*3)=95
95 % 10 = 5
So 2919-23-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H8O/c5-4-2-1-3-4/h4-5H,1-3H2

2919-23-5 Well-known Company Product Price

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  • Alfa Aesar

  • (A12430)  Cyclobutanol, 96%   

  • 2919-23-5

  • 1g

  • 447.0CNY

  • Detail
  • Alfa Aesar

  • (A12430)  Cyclobutanol, 96%   

  • 2919-23-5

  • 5g

  • 1146.0CNY

  • Detail
  • Alfa Aesar

  • (A12430)  Cyclobutanol, 96%   

  • 2919-23-5

  • 25g

  • 5731.0CNY

  • Detail

2919-23-5SDS

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 Cyclobutanol

1.2 Other means of identification

Product number -
Other names Hydroxy-cyclobutan

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:2919-23-5 SDS

2919-23-5Relevant articles and documents

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Meyer,K.,Rocek,J.

, p. 1209 - 1214 (1972)

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Thermal molecular beam matrix spectroscopy of cyclobutanol: temperature dependence of lineshapes and the conformation problem

Gunde, R.,Guenthard, Hs. H.

, p. 315 - 326 (1983)

Thermal molecular beam spectra of cyclobutanol isolated in Ar and Xe matrices and the temperature dependence of the ν(OH) Raman line are reported.Six matrix bands are shown by lineshape analysis to consist of 4-6 components which systematically decrease and increase with increasing temperature of the molecular beam source.Data on lineshape parameters and relative intensities are reported.Likewise the ν(OH) Raman band is shown to consist of four components which behave with respect to temperature dependence analogously to the matrix bands.The results will be discussed in terms of two models.

Ru-Photoredox-Catalyzed Decarboxylative Oxygenation of Aliphatic Carboxylic Acids through N-(acyloxy)phthalimide

Zheng, Chao,Wang, Yuting,Xu, Yangrui,Chen, Zhen,Chen, Guangying,Liang, Steven H.

supporting information, p. 4824 - 4827 (2018/08/24)

Decarboxylative aminoxylation of aliphatic carboxylic acid derivatives with (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) in the presence of ruthenium photoredox catalysis is reported. The key transformation entails a highly efficient photoredox catalytic cycle using Hantzsch ester as a reductant. The ensuing alkoxyamine can be readily converted to the corresponding alcohol in one pot, representing an alternative approach to access aliphatic alcohols under photoredox conditions.

Synthesis and kinetic regularities of the thermal decomposition of new hydrotrioxides of cyclic alcohols

Grabovskiy,Khalitova,Fedorova,Lobov,Rol’nik,Kabal’nova

, p. 464 - 468 (2017/03/08)

Cyclic hydrotrioxides were synthesized by low-temperature (?78 °C) ozonolysis of a series of cyclic alcohols and identified using 1H NMR spectra. The kinetic regularities of the thermal decomposition of the synthesized hydrotrioxides were studied. The experimental proof of the induced decomposition of alcohol hydrotrioxides was obtained for the first time using cyclohexanol hydrotrioxide as an example. The influence of cyclic substituents on the thermal stability of the hydrotrioxides is shown.

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