64246-13-5

Basic information

• Product Name: 1,1-bis[(1,3-benzodioxol-5-yloxy)methyl]-4-piperidin-1-ylbutyl acetate 2-hydroxypropane-1,2,3-tricarboxylate (salt)
• CAS NO: 64246-13-5
• Molecular Formula: C₃₃H₄₁NO₁₅
• Molecular Weight: 691.6763
• Mol File: 64246-13-5.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 630.4°C at 760 mmHg
• Flash Point: 335.1°C
• Vapor Pressure: 8.38E-16mmHg at 25°C
• CAS DataBase Reference: 1,1-bis[(1,3-benzodioxol-5-yloxy)methyl]-4-piperidin-1-ylbutyl acetate 2-hydroxypropane-1,2,3-tricarboxylate (salt)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-bis[(1,3-benzodioxol-5-yloxy)methyl]-4-piperidin-1-ylbutyl acetate 2-hydroxypropane-1,2,3-tricarboxylate (salt)(64246-13-5)
• EPA Substance Registry System: 1,1-bis[(1,3-benzodioxol-5-yloxy)methyl]-4-piperidin-1-ylbutyl acetate 2-hydroxypropane-1,2,3-tricarboxylate (salt)(64246-13-5)

Safety Data

• Hazardous Substances Data: 64246-13-5(Hazardous Substances Data)

Usage

Chemical structure

The compound has a complex structure with multiple functional groups, including a piperidine ring, a butyl acetate group, and a tricarboxylate salt.

Functional groups

The compound contains a piperidine ring, a butyl acetate group, and a tricarboxylate salt.

Aromatic rings

The compound includes benzodioxole moieties, which are aromatic rings containing oxygen atoms.

Pharmaceutical or industrial uses

Due to its complex structure and diverse functional groups, the compound is likely to have pharmaceutical or industrial uses.

Salt form

The compound is presented as a salt, which may affect its solubility and reactivity.

Molecular weight

The molecular weight of the compound is approximately 567.64 g/mol.

Stereochemistry

The compound may have stereoisomers due to the presence of chiral centers in the piperidine ring and butyl acetate group.

Stability

The stability of the compound may depend on factors such as temperature, pH, and the presence of other chemicals.

Reactivity

The compound may react with other chemicals, such as acids, bases, or nucleophiles, due to the presence of functional groups like the ester and carboxylate groups.