167482-99-7

Basic information

• Product Name: 5-(4-Carboxymethylphenyl)dipyrromethane (under argon)
• Synonyms: 5-(4-Carboxymethylphenyl)dipyrromethane (under argon);Methyl4-(Dipyrrol-2-yl)methylbenzoate
• CAS NO: 167482-99-7
• Molecular Formula: C₁₇H₁₆N₂O₂
• Molecular Weight: 280.32114
• Product Categories: Porphyrins
• Mol File: 167482-99-7.mol
• Article Data: 46

Chemical Properties

• Melting Point: 160-162 °C
• Boiling Point: 486.6±40.0 °C(Predicted)
• Appearance: /
• Density: 1.233±0.06 g/cm3(Predicted)
• PKA: 16.74±0.50(Predicted)
• CAS DataBase Reference: 5-(4-Carboxymethylphenyl)dipyrromethane (under argon)(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-Carboxymethylphenyl)dipyrromethane (under argon)(167482-99-7)
• EPA Substance Registry System: 5-(4-Carboxymethylphenyl)dipyrromethane (under argon)(167482-99-7)

Safety Data

• Hazardous Substances Data: 167482-99-7(Hazardous Substances Data)

Usage

Chemical compound

5-(4-Carboxymethylphenyl)dipyrromethane

Environment

Protected by argon gas

Structure

Dipyrromethane derivative with a carboxymethylphenyl group attached

Uses

Commonly used in organic chemistry for synthesis of complex molecules and materials

Applications

Potential applications in pharmaceuticals, materials science, and other scientific disciplines

Stability

Requires argon gas to ensure stability and prevent unwanted reactions with atmospheric oxygen or moisture

Upstream product

• 109-97-7 pyrrole 
• 1571-08-0 methyl 4-formylbenzoate 
• 1493817-13-2 4,4-difluoro-8-(4’-methoxycarbonylphenyl)-4-bora-3a,4a-diaza-s-indacene 
• 501326-94-9 5-(4-(methoxycarbonyl)phenyl)-4,6-dipyrrin 
• 619-66-9 4-Carboxybenzaldehyde 

Downstream Products

• 22220-19-5 5,10,15,20-tetrakis(1-undecyl)porphyrin 
• 22112-83-0 5,10,15,20-tetrakis(4-methoxycarbonylphenyl)porphyrin 
• 883455-85-4 (CH₃OC(O)C₆H₄C(C₄H₃N)2)(acetylacetonato)copper(II) 

Relevant articles and documents

Hydrogen bonding induced supramolecular self-assembly of linear doubly discotic triad supermolecules

A series of linear doubly discotic triad supermolecules based on a porphyrin (P) core and two triphenylene (Tp) arms linked by amide bonds are synthesized. The samples are denoted as P(Tp)2. Hydrogen bonding along the P stacks is the primary driving force

Photoconductivity in Metal–Organic Framework (MOF) Thin Films

Photoconductivity is a characteristic property of semi-conductors. Herein, we present a photo-conducting crystalline metal–organic framework (MOF) thin film with an on–off photocurrent ratio of two orders of magnitude. These oriented, surface-mounted MOF

Synthesis of phosphorescent asymmetrically π-extended porphyrins for two-photon applications

Significant effort has been directed in recent years toward porphyrins with enhanced two-photon absorption (2PA). However, the properties of their triplet states, which are central to many applications, have rarely been examined in parallel. Here we repor

MnIII(Porphyrin)-Based Porous Coordination Polymers: Synthesis, Catalytic Activities for the Oxidation of Ethylbenzene

Abstract: Six MnIII(porphyrin)-based porous coordination polymers, MnIII(F5CPp)–MnII (CP1, F5CPp=5-(pentafluorophenyl)-10,15,20-tri(4-carboxyphenyl)porphyrin dianion), MnIII(F5CP

Synthesis of 3,5-dichloro-4,4-difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPYs) via Cu(OTf)2 mediated oxidative nucleophilic substitution of hydrogen by chloride

Regioselective halogenation is often a key step in the formation of substituted 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) fluorophores, through the enablement of subsequent downstream C–C or C-X bond forming steps via SNAr or metal ca

Synthesis method of benzophenanthrene decyloxy bridged isooctyl alkoxy phenyl porphyrin ternary compound disc-like liquid crystal material

The invention discloses a synthesis method of benzophenanthrene decyloxy bridged isooctyl alkoxy phenyl porphyrin ternary compound disc-like liquid crystal material. The synthesis method comprises the following steps: firstly, performing synthesis to obta