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99498-65-4

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99498-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99498-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,4,9 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 99498-65:
(7*9)+(6*9)+(5*4)+(4*9)+(3*8)+(2*6)+(1*5)=214
214 % 10 = 4
So 99498-65-4 is a valid CAS Registry Number.

99498-65-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-3-(trifluoromethyl)pyrazole

1.2 Other means of identification

Product number -
Other names 1-phenyl-3-trifluoromethylpyrazole

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:99498-65-4 SDS

99498-65-4Relevant articles and documents

Exo/Endo Stereoselectivity in 1,3-Dipolar Cycloaddition of Trifluoroacetonitrile Oxide and -nitrilimine with Bicyclic Olefins

Tanaka, Kiyoshi,Masuda, Hideyuki,Mitsuhashi, Keiryo

, p. 3901 - 3904 (1986)

Trifluoroacetonitrile oxide and N-phenyl-C-(trifluoromethyl)nitrilimine cycloadded with norbornenes, resulting in the exclusive formation of the exo-adducts, while the concomitant formation of the endo-adducts was observed in their cycloadditions with nor

New strategy for the regioselective synthesis of 1-phenyl-3- trifluoromethyl-1H-pyrazoles

Zanatta, Nilo,Amaral, Simone S.,Dos Santos, Josiane M.,Da Silva, Andréia M.P.W.,Schneider, Juliana M.F.M.,Fernandes, Liana Da S.,Bonacorso, Helio G.,Martins, Marcos A.P.

, p. 4076 - 4079 (2013/07/25)

A regioselective synthesis of 3-trifluoromethyl-1-phenyl-1H-pyrazoles (1,3-isomers) as well as their 1,5-isomers (5-trifluoromethyl-1-phenyl-1H- pyrazoles), is described. The 1,3-isomers were obtained from the reaction of 4-alkoxy-1,1,1-trifluoroalk-3-en-2-ones with arylhydrazones followed by deprotective hydrolysis while the 1,5-isomer was obtained by direct cyclocondensation of 4-alkoxy-1,1,1-trifluoroalk-3-en-2-ones with phenylhydrazine. An unequivocal assignment of the 1,3- and 1,5-isomers of the pyrazole products is given.

Synergic effects of ionic liquid and microwave irradiation in promoting trifluoromethylpyrazole synthesis

Buriol, Lilian,Frizzo, Clarissa P.,Prola, Lizie D. T.,Moreira, Dayse N.,Marzari, Mara R. B.,Scapin, Elisandra,Zanatta, Nilo,Bonacorso, Helio G.,Martins, Marcos A. P.

experimental part, p. 1130 - 1135 (2012/06/18)

The synthesis of 5-trifluoromethyl-1-phenyl-1H-pyrazoles from the reactions of 4-alkoxy-1,1,1-trifluoro-3-alken-2-ones [CF3C(O)CH=C(R 1)OR, where R = Me, Et; R1= H, Me, Bu, i-Bu, Ph, 4-MeC6H4, 4-FCsu

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