104500-13-2

Basic information

• Product Name: 1,3-Propanediol, 2-((11H-benzo(b)fluoren-5-ylmethyl)amino)-2-methyl-, methanesulfonate (salt)
• Synonyms: 1,3-Propanediol, 2-((11H-benzo(b)fluoren-5-ylmethyl)amino)-2-methyl-, methanesulfonate (salt)
• CAS NO: 104500-13-2
• Molecular Formula: C23H27NO5S
• Molecular Weight: 0
• Mol File: 104500-13-2.mol

Chemical Properties

• Boiling Point: 606.6°Cat760mmHg
• Flash Point: 196.7°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 1.44E-15mmHg at 25°C
• CAS DataBase Reference: 1,3-Propanediol, 2-((11H-benzo(b)fluoren-5-ylmethyl)amino)-2-methyl-, methanesulfonate (salt)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Propanediol, 2-((11H-benzo(b)fluoren-5-ylmethyl)amino)-2-methyl-, methanesulfonate (salt)(104500-13-2)
• EPA Substance Registry System: 1,3-Propanediol, 2-((11H-benzo(b)fluoren-5-ylmethyl)amino)-2-methyl-, methanesulfonate (salt)(104500-13-2)

Safety Data

• Hazardous Substances Data: 104500-13-2(Hazardous Substances Data)

Usage

Molecular Structure

The compound has a 1,3-propanediol backbone with a 2-((11H-benzo(b)fluoren-5-ylmethyl)amino)-2-methylgroup attached to it.

Salt Form

The compound is in the form of a methanesulfonate salt.

Applications

The chemical may have various applications in industries such as pharmaceuticals, research, and manufacturing.

Unique Molecular Structure

The compound's unique molecular structure contributes to its potential applications and properties.

Chemical Properties

The specific chemical properties of the compound are not provided in the material, but they may include solubility, reactivity, and stability.

Potential Uses

The compound's unique structure and properties may make it useful in the development of new drugs, as a research tool, or in the manufacturing of various products.

Further Research

Further research may be needed to fully understand the compound's properties and potential applications.

InChI:InChI=1/C22H23NO2.CH4O3S/c1-22(13-24,14-25)23-12-20-18-8-4-2-6-15(18)10-17-11-16-7-3-5-9-19(16)21(17)20;1-5(2,3)4/h2-10,23-25H,11-14H2,1H3;1H3,(H,2,3,4)

Relevant articles and documents

Carbocyclic derivatives

The present invention relates to compounds of formula (I) or a monomethyl or monoethyl ether thereof (the compound of formula (I) including these ethers may contain no more than 30 carbon atoms in total); ethers, esters, thereof; acid addition salts thereof; wherein Ar is a C15-18 fused tetracarbocyclic ring system containing 3 or 4 aromatic rings or a C17-22 fused pentacarbocyclic ring system containing 4 or 5 aromatic rings, or a substituted derivative thereof; the ring system Ar being planar or deviating only slightly from planarity. Thus, the ring system contains a maximum of two non-aromatic carbon atoms which may be in the same ring, in which case they are adjacent, or in different rings; Ar is not perylene, fluoranthene, chrysene, pyrene, or triphenylene; R1 contains not more than eight carbon atoms and is a group STR1 wherein m is 0 or 1; R5 is hydrogen; R6 and R7 are the same or different and each is hydrogen or C1-5 alkyl optionally substituted by hydroxy; R8 and R9 are the same or different and each is hydrogen or C1-3 alkyl; STR2 is a five- or six-membered saturated carbocyclic ring; R10 is hydrogen, methyl or hydroxymethyl; R11, R12 and R13 are the same or different and each is hydrogen or methyl; R14 is hydrogen, methyl, hydroxy or hydroxymethyl.

Carbocyclic derivatives

The present invention relates to compounds of formula (I) or a monomethyl or monoethyl ether thereof (the compound of formula (I) including these ethers may contain no more than 30 carbon atoms in total); ethers, esters, thereof; acid addition salts thereof; wherein Ar is a C15-18 fused tetracarbocyclic ring system containing 3 or 4 aromatic rings or a C17-22 fused pentacarbocyclic ring system containing 4, or 5 aromatic rings, or a substituted derivative thereof; the ring system Ar should be planar or deviate only slightly from planarity. Thus, the ring system contains a maximum of two non-aromatic carbon atoms which may be in the same ring, in which case they are adjacent, or in different rings; Ar is not perylene, fluoranthene, chrysene, pyrene, or triphenylene; R1 contains not more than eight carbon atoms and is a group STR1 wherein m is 0 or 1; R5 is hydrogen; R6 and R7 are the same or different and each is hydrogen or C1-5 alkyl optionally substituted by hydroxy; R8 and R9 are the same or different and each is hydrogen or C1-3 alkyl; STR2 is a five- or six-membered saturated carbocyclic ring; R10 is hydrogen, methyl or hydroxymethyl; R11, R12 and R13 are the same or different and each is hydrogen or methyl; R14 is hydrogen, methyl, hydroxy, or hydroxymethyl.