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702650-29-1

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  • 1-[2-NITRO-4-(TRIFLUOROMETHYL)PHENYL]PIPERIDIN-4-OL

    Cas No: 702650-29-1

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702650-29-1 Usage

Chemical structure

The compound has a piperidine ring structure with a hydroxyl group attached to the 4th carbon atom.

Substituents

It contains a nitro group and a trifluoromethyl group on the 2nd and 4th positions of the phenyl ring, respectively.

Potential pharmaceutical applications

Due to its unique structure and substituents, the compound may have potential pharmaceutical applications.

Drug candidate

It may serve as a drug candidate for medical purposes, but further research and testing are required to determine its exact uses and effects.

Reactivity and toxicity

The compound should be handled and stored with care due to its potential for reactivity and toxicity.

Further research needed

The compound's potential uses and effects need to be determined through additional research and testing.

Check Digit Verification of cas no

The CAS Registry Mumber 702650-29-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,2,6,5 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 702650-29:
(8*7)+(7*0)+(6*2)+(5*6)+(4*5)+(3*0)+(2*2)+(1*9)=131
131 % 10 = 1
So 702650-29-1 is a valid CAS Registry Number.

702650-29-1Downstream Products

702650-29-1Relevant articles and documents

Nucleophilic aromatic substitution reactions under aqueous, mild conditions using polymeric additive HPMC

Ansari, Tharique N.,Borlinghaus, Niginia,Braje, Leon H.,Braje, Wilfried M.,Handa, Sachin,Ogulu, Deborah,Wittmann, Valentin

, p. 3955 - 3962 (2021)

The use of the inexpensive, benign, and sustainable polymer, hydroxypropyl methylcellulose (HPMC), in water enables nucleophilic aromatic subsitution (SNAr) reactions between various nucleophiles and electrophiles. The mild reaction conditions facilitate a broad functional group tolerance that can be utilized for subsequent derivatization for the synthesis of pharmaceutically relevant building blocks. The use of only equimolar amounts of all reagents and water as reaction solvent reveals the greenness and sustainability of the methodology presented herein.

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