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Benzenamine, 4-ethynyl-2,3,5,6-tetrafluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61794-59-0

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61794-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61794-59-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,9 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61794-59:
(7*6)+(6*1)+(5*7)+(4*9)+(3*4)+(2*5)+(1*9)=150
150 % 10 = 0
So 61794-59-0 is a valid CAS Registry Number.

61794-59-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethynyl-2,3,5,6-tetrafluoroaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,4-ethynyl-2,3,5,6-tetrafluoro

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:61794-59-0 SDS

61794-59-0Downstream Products

61794-59-0Relevant academic research and scientific papers

General and efficient synthesis of polyfluorinated 2-aminotolans and 2-arylindoles

Politanskaya, Larisa V.,Shteingarts, Vitalij D.,Tretyakov, Evgeny V.

, p. 85 - 98 (2016/07/19)

It was established here that cross-coupling of polyfluorinated 2-iodoanilines with arylacetylenes in MeCN in the presence catalytic amounts of Pd(PPh3)2Cl2, CuI and Et3N produces the corresponding 2-aminotolans although their yields are decreased from 98% to 40% with increasing fluorination of the substrates. It was shown that the 2-aminotolans with six or fewer fluorine atoms in their rings can be heterocyclised by heating in ethanol containing p-TSA to produce the corresponding polyfluorinated indoles. Cyclisation of tolans containing larger numbers of fluorine atoms in their rings proceeds most efficiently in the presence of KOH, resulting in 2-phenylindoles containing the current maximum of eight fluorine atoms.

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