1309569-29-6 Usage
Description
(2-Nitro-5-(pentafluorosulfanyl)phenyl)acetonitrile is a nitroaromatic chemical compound with the molecular formula C8H3F5N2O2S. It features a pentafluorosulfanyl group, which is highly electronegative and lipophilic, and is known for its strong electron-withdrawing properties. (2-Nitro-5-(pentafluorosulfanyl)phenyl)acetonitrile is utilized as a building block in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.
Uses
Used in Pharmaceutical Synthesis:
(2-Nitro-5-(pentafluorosulfanyl)phenyl)acetonitrile is used as a key intermediate in the development of pharmaceuticals due to its unique structural properties and reactivity in organic synthesis.
Used in Agrochemical Production:
(2-Nitro-5-(pentafluorosulfanyl)phenyl)acetonitrile serves as a building block in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural products.
Used in Fine Chemicals Synthesis:
(2-Nitro-5-(pentafluorosulfanyl)phenyl)acetonitrile is utilized in the production of fine chemicals, where its electron-withdrawing properties and reactivity are advantageous.
Used in Organic Reactions:
It is employed as a reactant in various organic reactions, including nucleophilic aromatic substitution, palladium-catalyzed cross-coupling reactions, and radical reaction processes, due to its strong electron-withdrawing nature.
Used as a Precursor in Dye and Pigment Synthesis:
The presence of the nitro group in (2-Nitro-5-(pentafluorosulfanyl)phenyl)acetonitrile makes it a potentially useful precursor in the synthesis of dyes, pigments, and fluorescent materials.
Safety Note:
It is crucial to handle (2-Nitro-5-(pentafluorosulfanyl)phenyl)acetonitrile with care, as it may present certain hazards if not used properly, given its reactivity and functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 1309569-29-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,5,6 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1309569-29:
(9*1)+(8*3)+(7*0)+(6*9)+(5*5)+(4*6)+(3*9)+(2*2)+(1*9)=176
176 % 10 = 6
So 1309569-29-6 is a valid CAS Registry Number.
1309569-29-6Relevant articles and documents
Synthesis of 5-pentafluorosulfanyl indazoles
Fan, Tao,Meng, Wei-Dong,Xiao, Yu-Lan,Zhang, Xingang
supporting information, p. 4473 - 4475 (2017/10/30)
An efficient method for the synthesis of 5-SF5 substituted indazoles from commercially available 4-nitro-(pentafluorosulfanyl)benzene through vicarious nucleophilic substitution of hydrogen (VNS) reaction, reduction of nitro group and cyclizati
Preparation of SF5 aromatics by vicarious nucleophilic substitution reactions of nitro(pentafluorosulfanyl)benzenes with carbanions
Beier, Petr,Pastyrikova, Tereza,Iakobson, George
experimental part, p. 4781 - 4786 (2011/07/07)
Vicarious nucleophilic substitutions (VNS) of hydrogen in 1-nitro-4-(pentafluorosulfanyl)benzene with carbanions provide 2-substituted 1-nitro-4-(pentafluorosulfanyl)benzenes in good to high yields. VNS of 1-nitro-3-(pentafluorosulfanyl)benzene gives a mi
