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5-(4-Bromophenyl)dipyrromethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 159152-11-1 Structure
  • Basic information

    1. Product Name: 5-(4-Bromophenyl)dipyrromethane
    2. Synonyms: 5-(4-Bromophenyl)dipyrromethane;4-(Dipyrrol-2-yl)methylbromobenzene
    3. CAS NO:159152-11-1
    4. Molecular Formula: C15H13BrN2
    5. Molecular Weight: 301.18112
    6. EINECS: N/A
    7. Product Categories: Porphyrins
    8. Mol File: 159152-11-1.mol
  • Chemical Properties

    1. Melting Point: 125-126 °C(Solv: ethanol (64-17-5); water (7732-18-5))
    2. Boiling Point: 474.8±40.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.465±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 16.81±0.50(Predicted)
    10. CAS DataBase Reference: 5-(4-Bromophenyl)dipyrromethane(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-(4-Bromophenyl)dipyrromethane(159152-11-1)
    12. EPA Substance Registry System: 5-(4-Bromophenyl)dipyrromethane(159152-11-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 159152-11-1(Hazardous Substances Data)

159152-11-1 Usage

General Description

5-(4-Bromophenyl)dipyrromethane is a chemical compound consisting of two pyrrole rings connected by a 4-bromophenyl group. It is commonly used in the synthesis of various porphyrin complexes, which have applications in fields such as medicine, catalysis, and materials science. 5-(4-Bromophenyl)dipyrromethane is known for its ability to form stable and reactive metal complexes, making it a valuable building block in the production of novel synthetic compounds. Additionally, 5-(4-Bromophenyl)dipyrromethane has been studied for its potential pharmaceutical properties, particularly in the field of photodynamic therapy for cancer treatment. Overall, its unique structure and reactivity make it a versatile and important component in the chemical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 159152-11-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,1,5 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 159152-11:
(8*1)+(7*5)+(6*9)+(5*1)+(4*5)+(3*2)+(2*1)+(1*1)=131
131 % 10 = 1
So 159152-11-1 is a valid CAS Registry Number.

159152-11-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-bromophenyl)-(1H-pyrrol-2-yl)methyl]-1H-pyrrole

1.2 Other means of identification

Product number -
Other names C-1927

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:159152-11-1 SDS

159152-11-1Relevant articles and documents

Dual emissive bodipy-benzodithiophene-bodipy TICT triad with a remarkable Stokes shift of 194 nm

Sengupta, Sanchita,Pandey, Upendra K.

, p. 2033 - 2038 (2018)

An acceptor-donor-acceptor (A-D-A) triad based on a BODIPY acceptor and a benzodithiophene donor exhibited dual fluorescence and pronounced fluorescence solvatochromism because of twisted intramolecular charge transfer (TICT) state formation. Furthermore,

Optical properties of two fluorene derived BODIPY molecular rotors as fluorescent ratiometric viscosity probes

Xochitiotzi-Flores, Elba,Jiménez-Sánchez, Arturo,García-Ortega, Héctor,Sánchez-Puig, Nuria,Romero-ávila, Margarita,Santillan, Rosa,Farfán, Norberto

, p. 4500 - 4512 (2016)

BODIPY-derived molecular fluorescent rotors are one of the most useful families of fluorescent probes for the quantitative measurement of microviscosity. Here, we report the photophysical properties of two molecular rotors as ratiometric viscosity sensors

A novel self-assembly based on double-layer zinc porphyrin sensitizers in supramolecular solar cell

Wu, Yu,Liu, Hua,Liu, Jia-Cheng,Li, Ren-Zhi,Jin, Neng-Zhi

, p. 69 - 82 (2019)

Two new self-assemblies based on zinc porphyrin dyes ZnPx-ZnPA (x = 1, 2) were synthesized and used for dye-sensitized solar cells. Capping layer dyes consist of zinc porphyrin (ZnP) as core unit and carbazole (P1), phenothiazine (P2) as electron-donating

Regioisomeric BODIPY Benzodithiophene Dyads and Triads with Tunable Red Emission as Ratiometric Temperature and Viscosity Sensors

Aswathy,Sharma, Sushil,Tripathi, Narendra Pratap,Sengupta, Sanchita

, p. 14870 - 14880 (2019)

Regioisomeric acceptor-donor (AD) molecular rotors (p-AD, m-AD and m-ADA) were synthesized and characterized, wherein dyads p-AD and m-AD, and triad m-ADA contained 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) and benzodithiophene (BDT) as electron-acceptor and electron-donor, respectively. In all the compounds, the donor and acceptor moieties are electronically decoupled by a phenyl spacer, either through a para coupling or through a meta coupling. The dyad counterparts p-AD and m-AD showed distinct photophysical characteristics in which dyad p-AD showed TICT band at ca. 654 nm characterized by a Stokes shift of ca. 150 nm and prominent solvatochromism. However, meta regioisomeric triad m-ADA showed well-defined aggregation in solution. Notably, because of the temperature-tunable and solvent-viscosity-dependent emission, efficient ratiometric temperature sensing with positive and negative temperature coefficients and viscosity sensing was observed for all compounds. Interestingly, the fluorescence of dyad m-AD (in 10/90 v/v THF/water) revealed a near-white light emission with CIE chromaticity coordinates (x, y) of (0.32, 0.29). Furthermore, the fluorescence emission of p-AD in THF at 0 °C also showed a near-white light emission with chromaticity coordinates (x, y) of (0.34, 0.27). Such multifunctional rotors with readily tunable emission in the red region and prominent temperature- and viscosity-sensing abilities are promising for sensing and bioimaging applications.

Ultrafast Charge-Separation in Triphenylamine-BODIPY-Derived Triads Carrying Centrally Positioned, Highly Electron-Deficient, Dicyanoquinodimethane or Tetracyanobutadiene Electron-Acceptors

Gautam, Prabhat,Misra, Rajneesh,Thomas, Michael B.,D'Souza, Francis

, p. 9192 - 9200 (2017)

A series of new triphenylamine (TPA)-substituted BODIPYs 1–3 have been designed and synthesized through the Pd-catalysed Sonogashira cross-coupling and [2+2] cycloaddition-retroelectrocyclization reactions in good yields. This procedure yielded highly ele

On the structure of meso-substituted F-BODIPYs and their assembly in molecular crystals: An experimental-theoretical approach

Xochitiotzi-Flores, Elba,Islas-Mejía, Alisul A.,García-Ortega, Héctor,Romero-ávila, Margarita,Mendez-Stivalet, José Manuel,Carreón-Castro, María Del Pilar,Santillan, Rosa,Maldonado-Domínguez, Mauricio,Arcos-Ramos, Rafael,Farfán, Norberto

, p. 148 - 157 (2016)

Molecular crystals of meso-(5-((4-formylphenyl)ethynyl)thiophen-2-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 4a and meso-(4-((4-formylphenyl)ethynyl)phenyl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 4b were synthesized using palladium(0)-catalyzed So

Syntheses and spectral properties of functionalized, water-soluble BODIPY derivatives

Li, Lingling,Han, Junyan,Nguyen, Binh,Burgess, Kevin

, p. 1963 - 1970 (2008)

(Chemical Equation Presented) The objective of this work was to form water-soluble 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) derivatives. Sulfonation conditions were developed for several BODIPY dyes to give the monosulfonated products 1a-3a and

Aluminum porphyrin complexes via delicate ligand design: Emerging efficient catalysts for high molecular weight poly(propylene carbonate)

Sheng, Xingfeng,Wang, Yong,Qin, Yusheng,Wang, Xianhong,Wang, Fosong

, p. 54043 - 54050 (2014)

Due to the deep concern over residual, toxic cobalt or chromium from catalysts in biodegradable poly(propylene carbonate) (PPC), bifunctional aluminum porphyrin complexes with quaternary ammonium salts anchored on the ligand framework were prepared, and a delicate design of the porphyrin ligand was obtained. An optimized catalyst was complex 6b, which had two para-bromine benzenes and two quaternary ammonium cations linked to benzene via a six-methylene spacer in the meso-position of the porphyrin framework and NO3- as axial ligand and quaternary ammonium anion, showed TOF of 560 h-1 at 80 °C and 3 MPa to yield PPC with 94% carbonate linkage and number average molecular weight of 96 kg mol-1. The PPC selectivity reached 93%, which was the highest record in this copolymerization for aluminum porphyrin complexes. The soil tolerant bifunctional aluminum porphyrin complexes are becoming increasingly competitive catalysts, since they can be left with the plastics without any extra separation. This journal is

Enhanced Electrocatalytic Activity of Thiophene-Substituted Asymmetric Porphyrin Film for Electrochemical Determination of Dopamine

Aysegul, Oksuz,Sadik, Cogal

, p. 2836 - 2843 (2020)

Abstract: Thiophene substituted porphyrin derivative was synthesized and investigated. The porphyrin derivative was characterized via MALDI-MS, 1H NMR, FT-IR, and cyclic voltammetry methods. The poly-porpyrin (PPor) film was electrochemically d

4-Carboxybiphenyl and thiophene substituted porphyrin derivatives for dye-sensitized solar cell

Cogal, Sadik,Erten-Ela, Sule,Ocakoglu, Kasim,Oksuz, Aysegul Uygun

, p. 87 - 95 (2016)

Porphyrin sensitizer (Por) containing 4-carboxybiphenyl and 2-thienyl and its metallated Zn(II) derivative (ZnPor) were synthesized and investigated. The porphyrin dyes were characterized by MALDI-MS, 1H NMR, UV–vis, fluorescence and cyclic vol

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