1312106-32-3

Basic information

• Product Name: 18-(nitrobenzylideneamino)phenylpiperidine-1-carboxylate
• Synonyms: 18-(nitrobenzylideneamino)phenylpiperidine-1-carboxylate
• CAS NO: 1312106-32-3
• Molecular Weight: 467.522
• Mol File: 1312106-32-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 18-(nitrobenzylideneamino)phenylpiperidine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: 18-(nitrobenzylideneamino)phenylpiperidine-1-carboxylate(1312106-32-3)
• EPA Substance Registry System: 18-(nitrobenzylideneamino)phenylpiperidine-1-carboxylate(1312106-32-3)

Safety Data

• Hazardous Substances Data: 1312106-32-3(Hazardous Substances Data)

Usage

Chemical class

Hetrocyclic organic compound

Structure

Derived from piperidine

Functional groups

Nitrobenzene and carboxylate

Potential applications

Pharmaceuticals and medicinal chemistry

Research status

Further research and testing needed

Unique properties

Unknown, but potentially significant due to its structure

Effects

Unknown, but may have potential uses in the medical field

Safety

Unknown, further testing needed to determine safety and potential side effects

Stability

Unknown, further testing needed to determine stability under various conditions

Solubility

Unknown, further testing needed to determine solubility in different solvents.

Upstream product

• 138229-59-1 3-formyl-2-nitrobenzoic acid methyl ester 
• 1171197-20-8 (3S)-3-(4-aminophenyl)piperidine-1-carboxylic acid tert-butyl ester 
• 875798-79-1 3-(4-aminophenyl)piperidine-1-carboxylic acid tert-butyl ester 
• 1196713-21-9 (3S)-3-(4-aminophenyl)piperidine 
• 4282-46-6 3-(4'-nitrophenyl)pyridine 
• 5471-82-9 methyl 3-methyl-2-nitrobenzoate 
• 19733-56-3 3-(4-aminophenyl)piperidine 
• 68109-89-7 β-(dimethylamino)-3-carbomethoxy-2-nitrostyrene 
• 1692-25-7 3-pyridylboronic acid 
• 586-78-7 para-nitrophenyl bromide 
• 132874-06-7 methyl 3-(bromomethyl)-2-nitrobenzoate 
• 171364-83-3 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nitrobenzene 
• 40114-49-6 1-benzyl-3-piperidone 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 1038915-64-8 (3S)-3-[4-[7-(aminocarbonyl)-2H-indazol-2-yl]phenyl]piperidinium chloride 
• 1196713-67-3 2-[4-((3S)-(tertbutoxycarbonyl)piperidin-3-yl)phenyl]-2H-indazole-7-carboxylic acid methyl ester 
• 1038916-08-3 2-{4-[(3S)-1-(tert-butoxycarbonyl)piperidin-3-yl]phenyl}-2H-indazole-7-carboxylic acid 
• 1038916-11-8 tert-butyl (3S)-3-{4-[7-(aminocarbonyl)-2H-indazol-2-yl]phenyl}piperidine-1-carboxylate 
• 1038915-60-4 (3S)-3-[4-{7-(aminocarbonyl)-2H-indazol-2-yl}phenyl]piperidine 

Relevant articles and documents

Derivative based on PARP inhibitor Niraparib and a preparation method and use thereof

The invention discloses a derivative based on a PARP inhibitor Niraparib. The derivative has a structure shown in a formula I as shown in the description, wherein R1 is selected from alkyl, alkoxy, cycloalkyl, aryl alkyl, cycloalkyl alkyl, heterocyclyl, a

A prepares Nepal to pull handkerchief Nepal method (by machine translation)

The invention discloses a compound 2 - [4 - ((3S) - 3 - piperidinyl) phenyl] - 2H - indazole - 7 - carboxamide preparation method, through the 4 - nitro phenylpyridyl with reaction produced animal pen halogenphenmethyl season ammonium salt, by sodium borohydride reduction of the pyridine quaternary ammonium salt, in the palladium reagent obtained under the action of the 3 - (4 - aminophenyl) piperidine, in the chiral reagent obtained under the action of the (S)- 3 - (4 - halophenyl) piperidine, with 3 - formyl - 2 - nitro-benzoic acid methyl ester condensation and in sodium azide formed under the action of powder medicine, after preparing the amine Niraparib (molecular entity is: 2 - [4 - ((3S) - 3 - piperidinyl) phenyl] - 2H - indazole - 7 - carboxamide). (by machine translation)