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58686-69-4

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58686-69-4 Usage

General Description

"(3-Trifluoromethyl-phenyl)-propynoic acid ethyl ester" is a chemical compound with the formula C11H11F3O2. It is an ethyl ester of propynoic acid with a trifluoromethyl-substituted phenyl group. (3-TRIFLUOROMETHYL-PHENYL)-PROPYNOIC ACID ETHYL ESTER is an organic compound with potential medicinal properties, and it may have applications in pharmaceutical research, particularly in the development of new drugs. Its precise properties and potential uses are still being explored, but it is a compound of interest in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 58686-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,8 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 58686-69:
(7*5)+(6*8)+(5*6)+(4*8)+(3*6)+(2*6)+(1*9)=184
184 % 10 = 4
So 58686-69-4 is a valid CAS Registry Number.

58686-69-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-[3-(trifluoromethyl)phenyl]prop-2-ynoate

1.2 Other means of identification

Product number -
Other names ethyl 3-trifluoromethylphenylpropiolate

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:58686-69-4 SDS

58686-69-4Relevant articles and documents

Ruthenium-catalyzed [2+2] cycloaddition reactions of a 2-oxa-3- azabicyclo[2.2.1]hept-5-ene with unsymmetrical alkynes

Durham, Robin,Mandel, Jeremie,Blanchard, Nicolas,Tam, William

scheme or table, p. 1494 - 1505 (2012/01/12)

Ruthenium-catalyzed [2+2] cycloaddition reactions of a 2-oxa-3- azabicyclo[2.2.1]hept-5-ene with unsymmetrical alkynes were investigated. Yields of up to 90% were obtained though regioselectivity was modest. Select cycloadducts could be separated and used to access a highly functionalized [3.2.0] bicyclic structure through reductive cleavage of the N-O bond. These ring-opened products displayed a chemical exchange phenomenon in 1D carbon NMR and required characterization by 2D NMR techniques.

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