7037-30-1

Basic information

• Product Name: 3-(1-METHYL-PIPERIDIN-4-YL)-PROPAN-1-OL
• Synonyms: 4-N-Methyl piperidine propanol;1-METHYL-4-PIPERIDINEPROPANOL
• CAS NO: 7037-30-1
• Molecular Formula: C₉H₁₉NO
• Molecular Weight: 157.2533
• Product Categories: Heterocycle-other series
• Mol File: 7037-30-1.mol

Chemical Properties

• Boiling Point: 222.928 °C at 760 mmHg
• Flash Point: 81.387 °C
• Appearance: /
• Density: 0.941g/cm³
• Vapor Pressure: 0.02mmHg at 25°C
• Refractive Index: 1.471
• Storage Temp.: 2-8°C
• PKA: 15.16±0.10(Predicted)
• CAS DataBase Reference: 3-(1-METHYL-PIPERIDIN-4-YL)-PROPAN-1-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(1-METHYL-PIPERIDIN-4-YL)-PROPAN-1-OL(7037-30-1)
• EPA Substance Registry System: 3-(1-METHYL-PIPERIDIN-4-YL)-PROPAN-1-OL(7037-30-1)

Safety Data

• Hazardous Substances Data: 7037-30-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
3-(1-Methyl-piperidin-4-yl)-propan-1-ol is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a valuable building block in the development of new drugs and medications.
Used in Chemical Research:
In the field of chemical research, 3-(1-Methyl-piperidin-4-yl)-propan-1-ol serves as a subject for studying the properties and behavior of piperidine derivatives. This can lead to a better understanding of their potential applications and interactions with other chemical entities.
Used in Material Science:
3-(1-Methyl-piperidin-4-yl)-propan-1-ol may be utilized in the development of new materials with specific properties, such as improved solubility or reactivity. Its incorporation into polymers or other materials could result in novel applications in various industries.

InChI:InChI=1/C9H19NO/c1-3-9(11)8-4-6-10(2)7-5-8/h8-9,11H,3-7H2,1-2H3

Upstream product

• 2629-72-3 4-(3-Hydroxypropyl)pyridine 
• 50-00-0 formaldehyd 
• 154775-43-6 3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propanoic acid 
• 108153-26-0 4-(3-hydroxy-propyl)-1-methyl-pyridinium; bromide 
• 7037-49-2 3-(piperidin-4-yl)propan-1-ol 

Downstream Products

• 622369-21-5 4-[(2,4-dichloro-5-methoxyphenyl)amino]-6-methoxy-7-[3-(1-methylpiperidin-4-yl)propoxy]quinoline-3-carbonitrile 
• 1202680-04-3 N-[3-(1-methylpiperidin-4-yl)-propyl]-N,N'-di-cbz-guanidine 
• 753005-93-5 4-[(2,4-dichloro-5-methoxyphenyl)amino]-6-ethoxy-7-[3-(1-methylpiperidin-4-yl)propoxy]quinoline-3-carbonitrile 
• 848847-25-6 2-chloro-4-[3-(1-methyl-piperidin-4-yl)-propoxy]-benzaldehyde 
• 857385-32-1 2-cyclohexyl-5-(1-methyl-[4]piperidyl)-2-phenyl-valeronitrile 
• 857377-15-2 4-(4-cyclohexyl-4-phenyl-butyl)-1-methyl-piperidine 

Relevant articles and documents

Process for the preparation of substituted pyrimidine derivatives

The present invention is directed to processes for the preparation of substituted pyrimidine derivatives, useful as intermediates in the synthesis of histamine H4 receptor modulators, and to intermediates in H4 modulator synthesis.

[4-(Benzo[B]Thiophen-2-Yl) Pyrimidin-2-Yl]-Amine Derivatives As Ikk-Beta Inhibitors For The Treatment Of Cancer And Inflammatory Diseases

The present invention provides compounds of Formula I: useful in the treatment of cancer and inflammatory diseases.

Benzoimidazole compounds

Benzoimidazole compounds, compositions, and methods of using them in leukocyte recruitment inhibition, in modulating H4 receptor, and in treating conditions such as inflammation, H4 receptor-mediated conditions, and related conditions.

Imidazole compounds

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