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890147-29-2

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890147-29-2 Usage

Nitrile compound

Presence of a cyanide group (C≡N)
2-(4-fluorobenzyl)-3-hydroxy propanenitrile contains a cyanide group, which is a strong electronegative group that can participate in various chemical reactions.

Hydroxyl group

Presence of an -OH group
This compound has a hydroxyl group, which is a polar functional group that can form hydrogen bonds and participate in various chemical reactions.

Fluorobenzyl substitution

Presence of a 4-fluorophenyl group attached to the benzyl moiety
The presence of a fluorine atom on the benzyl ring influences the compound's reactivity, stability, and lipophilicity, which can be important in medicinal chemistry applications.

Potential applications

Organic synthesis and medicinal chemistry
2-(4-fluorobenzyl)-3-hydroxy propanenitrile may be used as a building block for the synthesis of various pharmaceutical drugs and other biologically active compounds.

Context-dependent properties

Properties and uses may vary based on specific conditions and context
The precise properties and potential uses of 2-(4-fluorobenzyl)-3-hydroxy propanenitrile may change depending on the specific context in which it is used, such as the presence of other chemicals or reaction conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 890147-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,0,1,4 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 890147-29:
(8*8)+(7*9)+(6*0)+(5*1)+(4*4)+(3*7)+(2*2)+(1*9)=182
182 % 10 = 2
So 890147-29-2 is a valid CAS Registry Number.

890147-29-2Relevant articles and documents

Synthesis of multifunctional polymer containing Ni-Pd NPs via thiol-ene reaction for one-pot cascade reactions

Javad Kalbasi, Roozbeh,Mesgarsaravi, Niloofar,Gharibi, Reza

, (2019)

Recently, acid–base bifunctional catalysts have been considered due to their abilities, such as the simultaneous activation of electrophilic and nucleophilic species and their high importance in organic syntheses. However, the synthesis of acid–base catalysts is problematic due to the neutralization of acidic and basic groups. This work reports a facial approach to solve this problem via the synthesis of a novel bifunctional polymer using inexpensive materials and easy methods. In this way, at the first step, heterogeneous poly (styrene sulfonic acid-n-vinylimidazole) containing pentaerythritol tetra-(3-mercaptopropionate) (PETMP) and trimethylolpropane trimethacrylate (TMPTMA) cross-linkers were synthesized in the pores of a mesoporous silica structure using click reaction as a novel bifunctional acid–base catalyst. After that, Ni-Pd nanoparticles supported on poly (styrenesulfonic acid-n-vinylimidazole)/KIT-6 as a novel trifunctional heterogeneous acid–base-metal catalyst was prepared. The prepared catalysts were characterized by various techniques like FT-IR, TGA, ICP-AES, DRS-UV, TEM, FE-SEM, EDS-Mapping, and XRD. The synthesized catalysts were efficiently used as bifunctional/trifunctional catalysts for one-pot, deacetalization-Knoevenagel condensation and one-pot, three-step and a sequential reaction containing deacetalization-Knoevenagel condensation-reduction reaction. It is important to note that the synthesized catalyst showing high chemo-selectivity for the reduction of nitro group, alkenyl double bond and ester group in the presence of nitrile. Moreover, it was found that the different nanoparticles including Ni, Pd, and alloyed Ni-Pd showing different chemo-selectivity and catalytic activity in the reaction.

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