1236303-09-5 Usage
General Description
Methyl 2-iodo-4-(trifluoromethyl)benzoate is a chemical compound with the molecular formula C9H6F3IO2. It is a highly reactive and potentially hazardous compound that is commonly used in organic synthesis. Methyl 2-iodo-4-(trifluoromethyl)benzoate is often employed as a reagent in the preparation of various pharmaceuticals and agrochemicals due to its ability to facilitate carbon-carbon bond formation. It is also utilized in the production of specialized materials such as liquid crystals and polymers. However, caution should be exercised when handling this compound, as it is toxic and may pose environmental risks if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 1236303-09-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,6,3,0 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1236303-09:
(9*1)+(8*2)+(7*3)+(6*6)+(5*3)+(4*0)+(3*3)+(2*0)+(1*9)=115
115 % 10 = 5
So 1236303-09-5 is a valid CAS Registry Number.
1236303-09-5Relevant articles and documents
F- Nucleophilic-Addition-Induced [3 + 2] Annulation: Direct Access to CF3-Substituted Indenes
Tang, Hai-Jun,Zhang, Yu-Feng,Jiang, Yi-Wen,Feng, Chao
supporting information, p. 5190 - 5193 (2018/09/12)
An efficient [3 + 2] annulation of (2,2-difluorovinyl)-2-iodoarenes and internal alkynes was developed for the synthesis of 1-(trifluoromethyl)-1H-indenes. The success of this strategy hinges upon a well-balanced process for the generation of two transient reactive species, specifically trifluoroethylsilver and alkenylpalladium intermediates, in the same molecule, as well as a smooth transmetalation step, which delicately joins together these two different metallic intermediates.
PIPERIDINE DERIVATIVES
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Page/Page column 31, (2010/08/08)
The present invention relates to a compound of formula I wherein R1, R2, and Ar are as defined herein or to a pharmaceutically acceptable acid addition salt, to a racemic mixture, or to its corresponding enantiomer and/or optical iso