61020-07-3

Basic information

• Product Name: 2-METHOXY-1-FORMYLPIPERIDINE
• Synonyms: N-FORMYL-2-METHOXY-PIPERIDINE;2-METHOXY-1-FORMYLPIPERIDINE;2-Methoxypiperidine-1-carboxaldehyde;N-FORMYL-2-METHOXY-PIPERIDINE 97%;1-Piperidinecarboxaldehyde, 2-methoxy- (9CI);N-Methoxy-1-formylpiperidine;2-METHOXY-1-PIPERIDINECARBOXALDEHYDE;2-Methoxy-1-piperidinecarbaldehyde
• CAS NO: 61020-07-3
• Molecular Formula: C₇H₁₃NO₂
• Molecular Weight: 143.18
• Product Categories: ALDEHYDE
• Mol File: 61020-07-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 261.28°C (rough estimate)
• Flash Point: 98.9°C
• Appearance: /
• Density: 1.0500
• Vapor Pressure: 0.0197mmHg at 25°C
• Refractive Index: 1.4610 (estimate)
• CAS DataBase Reference: 2-METHOXY-1-FORMYLPIPERIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHOXY-1-FORMYLPIPERIDINE(61020-07-3)
• EPA Substance Registry System: 2-METHOXY-1-FORMYLPIPERIDINE(61020-07-3)

Safety Data

• Safety Statements: S24/25:Avoid contact with skin and eyes.
• Hazardous Substances Data: 61020-07-3(Hazardous Substances Data)

Usage

Chemical Properties

CLEAR COLOURLESS LIQUID

InChI:InChI=1/C7H13NO2/c1-10-7-4-2-3-5-8(7)6-9/h6-7H,2-5H2,1H3/t7-/m0/s1

Upstream product

• 2591-86-8 N-Formylpiperidine 
• 67-56-1 methanol 

Downstream Products

• 80574-60-3 N-formyl-2-(2,5-dimethylphenyl)-piperidine 
• 133535-64-5 2-(phenylsulphonyl)-1-piperidinecarboxaldehyde 
• 80574-71-6 N-formyl-2-(2,5-dimethoxyphenyl)-piperidine 
• 80574-62-5 N-formyl-2-(2,4,6-trimethylphenyl)-piperidine 
• 71602-40-9 2-phenyl-1-piperidinecarboxaldehyde 
• 19615-30-6 piperidin-2-yl-acetic acid hydrochloride 
• 68291-31-6 2-ethyl-1-piperidinecarboxaldehyde 
• 81097-36-1 1-(toluene-4-sulfonyl)-1,2,3,4-tetrahydropyridine 
• 134415-12-6 1-<(4-methylphenyl)sulphonyl>-2-(phenylsulphonyl)piperidine 
• 2591-86-8 N-Formylpiperidine 

Relevant articles and documents

Stereoselective synthesis of 3-deoxy-piperidine iminosugars from l-lysine

A new method using electrochemical oxidation and/or OsO4 oxidation has been used for the stereoselective synthesis of 2,3,6-trihydroxylated (5S)-piperidine derivatives. The electrochemical method was successively used for the conversion of N-pr

Electro-organic Reactions. Part 23. Regioselectivity and the Stereochemistry of Anodic Methoxylation of N-Acylpiperidines and N-Acylmorpholines

Anodic methoxylation of conformationally biassed N-acylpiperidines has been shown to give axial substitution due to steric constraints imposed by relatively slow rotation of the planar N-acyl groups.These steric constraints also account for the regioselec