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Acetic acid, trifluoro-, (4-nitrophenyl)methyl ester, also known as trifluoroacetic acid 4-nitrobenzyl ester, is a chemical compound with the molecular formula C9H7F3NO4. It is a colorless to pale yellow liquid with a molecular weight of 259.15 g/mol. This ester is synthesized by the reaction of trifluoroacetic acid with 4-nitrobenzyl alcohol, and it is used as a reagent in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. The compound is sensitive to moisture and should be stored under anhydrous conditions. Due to its reactivity and potential hazards, it is essential to handle this chemical with proper safety precautions and in accordance with relevant regulations.

405-84-5

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405-84-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 405-84-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 405-84:
(5*4)+(4*0)+(3*5)+(2*8)+(1*4)=55
55 % 10 = 5
So 405-84-5 is a valid CAS Registry Number.

405-84-5Relevant academic research and scientific papers

Palladium-catalyzed, asymmetric Mizoroki-Heck reaction of benzylic electrophiles using phosphoramidites as chiral ligands

Yang, Zhigang,Zhou, Jianrong

supporting information; experimental part, p. 11833 - 11835 (2012/09/08)

We report herein the first examples of asymmetric Mizoroki-Heck reactions using benzyl electrophiles. A new phosphoramidite was identified to be an effective chiral ligand in the palladium-catalyzed reaction. The reaction is compatible with polar functional groups and can be readily scaled up. Several cyclic olefins worked well as olefin components. Thirty-one examples are included.

A one-pot rapid synthesis of dithiocarbamates from alcohols using a polymer supported diethyl dithiocarbamate anion

Bandgar,Sadavarte,Uppalla

, p. 450 - 451 (2007/10/03)

A polymer supported diethyl dithiocarbamate anion reacts with primary and secondary alcohols via their tirfluoracetates giving alkylated diethyl dithiocarbamates in good yields.

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