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2-(4-methoxyphenyl)-5-trifluoroacetylpyrrole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91735-79-4

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91735-79-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91735-79-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,3 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91735-79:
(7*9)+(6*1)+(5*7)+(4*3)+(3*5)+(2*7)+(1*9)=154
154 % 10 = 4
So 91735-79-4 is a valid CAS Registry Number.

91735-79-4Relevant academic research and scientific papers

Synthesis and optical properties of difluorobora-s-diazaindacene dyes with trifluoromethyl meso-substituents

Sobenina, Lyubov N.,Petrova, Olga V.,Petrushenko, Konstantin B.,Ushakov, Igor A.,Mikhaleva, Albina I.,Meallet-Renault, Rachel,Trofimov, Boris A.

, p. 4107 - 4118 (2013/07/19)

A series of meso-CF3-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) dyes with aryl and hetaryl substituents at the C-3 and C-5 positions, both symmetric and asymmetric, have been synthesized in 36-90 % yields by a new strategy involving as the key step the condensation of 2,2,2-trifluoro-1-(5- arylpyrrol-2-yl)-1-ethanols with diverse 2-arylpyrroles. The starting 2,2,2-trifluoro-1-(5-arylpyrrol-2-yl)-1-ethanols are easily prepared by reduction of the available 2-trifluoroacetyl-5-arylpyrroles. The synthesized dyes fluoresce in a longer wavelength region (626-698 nm) with high quantum yield (0.84-0.99). A new strategy for the synthesis of highly efficient symmetric and asymmetric BODIPY fluorophores that combine trifluoromethyl and 3,5-aryl substituents has been developed. The key step is the P 2O5-promoted condensation of 2,2,2-trifluoro-1-(5- arylpyrrol-2-yl)-1-ethanols with diverse 2-arylpyrroles. Copyright

PYRROLES FROM KETOXIMES AND ACETYLENE. 38. NEW REPRESENTATIVES OF TRIFLUOROACETYLPYRROLES. SYNTHESIS AND TRANSFORMATIONS

Korostova, S. E.,Mikhaleva, A. I.,Sobenina, L. N.,Shevchenko, S. G.,Sigalov, M. V.,et al.

, p. 39 - 43 (2007/10/02)

A series of previously unknown trifluoroacetyl derivatives of pyrroles were obtained with high yields by the reaction of pyrroles, including N-vinyl-substituted pyrroles, with trifluoroacetic anhydride in the presence of pyridine at room temperature.The s

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