945632-52-0

Basic information

• Product Name: 1,3-Propanediol, 2-aMino-2-(1,2,3,4-tetrahydro-6-octyl-2-naphthalenyl)-
• Synonyms: 1,3-Propanediol, 2-aMino-2-(1,2,3,4-tetrahydro-6-octyl-2-naphthalenyl)-;2-Amino-2-(6-octyl-1,2,3,4-tetrahydronaphthalen-2-yl)propane-1,3-diol
• CAS NO: 945632-52-0
• Molecular Formula: C21H35NO2
• Molecular Weight: 333.5081
• Mol File: 945632-52-0.mol

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1,3-Propanediol, 2-aMino-2-(1,2,3,4-tetrahydro-6-octyl-2-naphthalenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Propanediol, 2-aMino-2-(1,2,3,4-tetrahydro-6-octyl-2-naphthalenyl)-(945632-52-0)
• EPA Substance Registry System: 1,3-Propanediol, 2-aMino-2-(1,2,3,4-tetrahydro-6-octyl-2-naphthalenyl)-(945632-52-0)

Safety Data

• Hazardous Substances Data: 945632-52-0(Hazardous Substances Data)

Usage

Derivative of 1,3-propanediol

Yes
The compound is derived from 1,3-propanediol, which is a colorless, odorless, and slightly viscous liquid.

Parent compound

1,3-propanediol
The parent compound is a common ingredient in the production of polymers and cosmetics.

Addition of 2-amino-2-(1,2,3,4-tetrahydro-6-octyl-2-naphthalenyl) group

Yes
The addition of this group to the 1,3-propanediol molecule introduces an aromatic ring and an amine functional group.

Aromatic ring

Present
The presence of an aromatic ring in the molecule may contribute to its chemical reactivity and stability.

Amine functional group

Present
The amine functional group can participate in various chemical reactions, such as acid-base reactions, nucleophilic substitution, and electrophilic addition.

Potential applications

Pharmaceuticals, organic synthesis, and material science
The compound may have applications in these fields due to its unique chemical structure and properties.

Chemical reactivity

May vary
The reactivity of the compound depends on the specific reactions and conditions it is subjected to, influenced by the presence of the aromatic ring and amine functional group.

Physical properties

Unknown
The physical properties, such as color, odor, and viscosity, are not provided in the material but may be influenced by the presence of the aromatic ring and amine functional group.

Stability

Unknown
The stability of the compound under various conditions is not provided in the material but may be affected by the presence of the aromatic ring and amine functional group.

Upstream product

• 144464-64-2 5-oxo-5,6,7,8-tetrahydronaphthalen-2-yl trifluoromethanesulfonate 
• 3470-50-6 6-Hydroxy-1-tetralone 
• 945632-79-1 2-acetylamino-2-(6-octyl-1-oxo-1,2,3,4-tetrahydro-naphthalen-2-yl)-malonic acid diethyl ester 
• 945632-81-5 2-acetylamino-2-(6-octyl-1,2,3,4-tetrahydro-naphthalen-2-yl)-malonic acid diethyl ester 
• 945632-77-9 2-bromo-6-octyl-3,4-dihydro-2H-naphthalen-1-one 
• 945632-75-7 6-octyl-3,4-dihydro-2H-naphthalen-1-one 
• 1118948-68-7 N-[2-hydroxy-1-hydroxymethyl-1-(6-octyl-1,2,3,4-tetrahydro-naphthalen-2-yl)ethyl]-acetamide 

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Compounds that have agonist activity at one or more of the S1P receptors are provided. The compounds are sphingosine analogs that, after phosphorylation, can behave as agonists at S1P receptors.