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1H-Tetrazole, 1-(4-methylphenyl)-5-(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129191-84-0

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129191-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129191-84-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,1,9 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 129191-84:
(8*1)+(7*2)+(6*9)+(5*1)+(4*9)+(3*1)+(2*8)+(1*4)=140
140 % 10 = 0
So 129191-84-0 is a valid CAS Registry Number.

129191-84-0Downstream Products

129191-84-0Relevant academic research and scientific papers

Synthesis of trifluoromethyltetrazoles via building block strategy

Xiao, Jingbo,Zhang, Xiaomei,Wang, Deying,Yuan, Chengye

, p. 83 - 85 (1999)

A series of 1-substituted-5-trifluoromethyltetrazoles was conveniently prepared from N-substituted trifluoroacetimidoyl chlorides via nucleophilic replacement with azide anion followed by subsequent cyclization in moderate to excellent yield by building b

Microwave-assisted synthesis of 1-aryl-5-(trifluoromethyl)-1H-tetrazoles

Rahmani, Fariba,Darehkordi, Ali,Notash, Behrouz

, p. 84 - 87 (2014/10/15)

This general protocol provides a wide variety of 5-substituted-1H- tetrazoles in good yields under mild reaction conditions. An efficient, green, and convenient method for the preparation of new 5-substituted-tetrazoles via microwave-assisted 1,3-dipolar cycloaddition reaction of N-aryl-2,2,2- trifluoroacetimidoyl chlorides and sodium azide in acetonitrile without assistance of any catalyst has been reported. The FT-IR, 19F NMR, 1H NMR, 13C NMR, HMBC spectra, elemental analysis, and single-crystal X-ray analysis confirm the structures of the products.

Microwave-assisted synthesis of 1-aryl-5-(trifluoromethyl)-1H-tetrazoles

Rahmani, Fariba,Darehkordi, Ali,Notash, Behrouz

, p. 84 - 87 (2014/12/10)

This general protocol provides a wide variety of 5-substituted-1H-tetrazoles in good yields under mild reaction conditions. An efficient, green, and convenient method for the preparation of new 5-substituted-tetrazoles via microwave-assisted 1,3-dipolar cycloaddition reaction of N-aryl-2,2,2-trifluoroacetimidoyl chlorides and sodium azide in acetonitrile without assistance of any catalyst has been reported. The FT-IR, 19F NMR, 1H NMR, 13C NMR, HMBC spectra, elemental analysis, and single-crystal X-ray analysis confirm the structures of the products.

PROCESS FOR PRODUCTION OF 1-ARYL-5-(TRIFLUOROMETHYL)-1H- TETRAZOLES

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Page/Page column 6, (2008/06/13)

The present invention relates to a process for producing an N-aryl-2,2,2-trifluoroacetimidoyl chloride represented by Formula (2): the process comprising the step of reacting in an organic solvent a tertiary amine, a 2,2,2-trifluoro-N-arylacetamide repre

N,N'-Disubstituted trifluoroacetamidines for trifluoromethylated polynitrogen heterocycles

Uneyama,Yamashita,Sugimoto,Morimoto

, p. 2717 - 2718 (2007/10/02)

N,N'-Disubstituted trifluoroacetamidines have been prepared and transformed to the trifluoromethylated polynitrogen heterocycles.

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