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26458-04-8

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26458-04-8 Usage

Synthesis Reference(s)

Tetrahedron Letters, 32, p. 7689, 1991 DOI: 10.1016/0040-4039(91)80566-O

Check Digit Verification of cas no

The CAS Registry Mumber 26458-04-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,4,5 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 26458-04:
(7*2)+(6*6)+(5*4)+(4*5)+(3*8)+(2*0)+(1*4)=118
118 % 10 = 8
So 26458-04-8 is a valid CAS Registry Number.

26458-04-8 Well-known Company Product Price

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  • Aldrich

  • (737186)  1-(Trifluoromethyl)naphthalene  95%

  • 26458-04-8

  • 737186-1G

  • 1,093.95CNY

  • Detail

26458-04-8SDS

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 1-(trifluoromethyl)naphthalene

1.2 Other means of identification

Product number -
Other names 1-Trifluoromethyl-naphthalene

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:26458-04-8 SDS

26458-04-8Relevant articles and documents

Merging visible-light photocatalysis and transition-metal catalysis in the copper-catalyzed trifluoromethylation of boronic acids with CF3I

Ye, Yingda,Sanford, Melanie S.

supporting information; experimental part, p. 9034 - 9037 (2012/07/13)

This communication describes the development of a mild method for the cross-coupling of arylboronic acids with CF3I via the merger of photoredox and Cu catalysis. This method has been applied to the trifluoromethylation of electronically diverse aromatic and heteroaromatic substrates and tolerates many common functional groups.

Copper electron-transfer induced trifluoromethylation with methyl fluorosulphonyldifluoroacetate

Chen, Qing-Yun,Yang, Guo-Ying,Wu Sheng-Wen

, p. 291 - 298 (2007/10/02)

Treatment of halogen compounds, RX, with methyl fluorosulfonyldifluoroacetate and copper powder in dimethylformamide for 4 h at 65 - 80 deg C resulted in the corresponding trifluoromethylated products, RCF3, in good yield.In the absence of halogen compounds and at 100 deg C, methyl triflone (CF3SO2CH3) was synthesized readily in the 20 - 30percent yield from the same reaction system.The fact that the reaction was suppressed by oxygen, p-dinitrobenzene or in the darkness suggested that a copper-induced electron-transfer process was involved in this new trifluoromethylating system.

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