306296-69-5 Usage
Physical State
Colorless liquid
Usage
Commonly used in the synthesis of pharmaceuticals and agrochemicals
Application
Potential applications in the field of organic synthesis
Specific Use
Reagent for the introduction of the trifluoromethoxy group into various organic compounds
Safety Precaution
Should be handled and used with caution
Health Hazards
Potential health hazards associated with its use
Environmental Impact
Potential environmental impact due to its chemical properties
Chemical Structure
Contains a benzene ring with a chloroethyl group at the 1st position and a trifluoromethoxy group at the 4th position.
Check Digit Verification of cas no
The CAS Registry Mumber 306296-69-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,6,2,9 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 306296-69:
(8*3)+(7*0)+(6*6)+(5*2)+(4*9)+(3*6)+(2*6)+(1*9)=145
145 % 10 = 5
So 306296-69-5 is a valid CAS Registry Number.
306296-69-5Relevant articles and documents
Nickel-catalyzed asymmetric reductive cross-coupling between vinyl and benzyl electrophiles
Cherney, Alan H.,Reisman, Sarah E.
supporting information, p. 14365 - 14368 (2014/12/11)
A Ni-catalyzed asymmetric reductive cross-coupling between vinyl bromides and benzyl chlorides has been developed. This method provides direct access to enantioenriched products bearing aryl-substituted tertiary allylic stereogenic centers from simple, stable starting materials. A broad substrate scope is achieved under mild reaction conditions that preclude the pregeneration of organometallic reagents and the regioselectivity issues commonly associated with asymmetric allylic arylation.
