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

167482-99-7

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167482-99-7 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

Check Digit Verification of cas no

The CAS Registry Mumber 167482-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,4,8 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 167482-99:
(8*1)+(7*6)+(6*7)+(5*4)+(4*8)+(3*2)+(2*9)+(1*9)=177
177 % 10 = 7
So 167482-99-7 is a valid CAS Registry Number.

167482-99-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 4-(Dipyrrol-2-yl)methylbenzoate

1.2 Other means of identification

Product number -
Other names -

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:167482-99-7 SDS

167482-99-7Relevant articles and documents

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

Miao, Jianjun,Zhu, Lei

, p. 1634 - 1641 (2010)

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

2D porphyrinic metal-organic frameworks featuring rod-shaped secondary building units

Aggarwal, Aviral,Elliott, Rory,Ryan, Aoife A.,Schmitt, Wolfgang,Senge, Mathias O.,Steuber, Friedrich W.,Zhu, Nianyong

, (2021)

Metal-organic frameworks (MOFs) encompass a rapidly expanding class of materials with diverse potential applications including gas storage, molecular separation, sensing and catalysis. So-called ‘rod MOFs’, which comprise infinitely extended 1D secondary

Photoconductivity in Metal–Organic Framework (MOF) Thin Films

Liu, Xiaojing,Kozlowska, Mariana,Okkali, Timur,Wagner, Danny,Higashino, Tomohiro,Brenner-Wei?, Gerald,Marschner, Stefan M.,Fu, Zhihua,Zhang, Qiang,Imahori, Hiroshi,Br?se, Stefan,Wenzel, Wolfgang,W?ll, Christof,Heinke, Lars

, p. 9590 - 9595 (2019)

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

Raman spectroscopy of dipyrrins: Nonresonant, resonant and surface-enhanced cross-sections and enhancement factors

McLean, Tracey M.,Cleland, Deidre,Gordon, Keith C.,Telfer, Shane G.,Waterland, Mark R.

, p. 2154 - 2164 (2011)

Detailed studies of the mechanism of surface-enhanced (resonance) Raman spectroscopy (SE(R)RS), and its applications, place a number of demands on the properties of SERS scatterers. With large Raman cross-sections, versatile synthetic chemistry and comple

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

Esipova, Tatiana V.,Vinogradov, Sergei A.

, p. 8812 - 8825 (2014)

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

A photoactive molecular triad as a nanoscale power supply for a supramolecular machine

Saha, Sourav,Johansson, Erik,Flood, Amar H.,Tseng, Hsian-Rong,Zink, Jeffrey I.,Stoddart, J. Fraser

, p. 6846 - 6858 (2005)

A tetrathiafulvalene-porphyrin-fullerene (TTF-P-C60) molecular triad, which generates electrical current by harnessing light energy when self-assembled onto gold electrodes, has been developed. The triad, composed of three unique electroactive

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

Sun, Shu,Pan, Mi,Hu, Xiaodong,Shao, Weihao,Li, Jun,Zhang, Fengxing

, p. 1087 - 1098 (2016)

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

Convergent synthesis of meso-ferrocenyl porphyrins for TiO2 sensitization

Harney, Joseph P.,Dransfield, Timothy,Rochford, Jonathan

, p. 4700 - 4703 (2012)

Electron-donating ferrocenyl moieties have been incorporated into supramolecular carboxyporphyrin architectures Zn(II)-5-ferrocenyl-10,20- bistolyl-15-(4-methylbenzoate)porphyrin (trans-Fc-ZnP-CO2Me), Zn(II)-5-ferrocenyl-10,15,20-tris(4-methylbenzoate)porphyrin [trans-Fc-ZnP-(CO2Me)3], and Zn(II)-5,15-bisferrocenyl-10, 20-bis(4-benzoate)porphyrin [trans-Fc2-ZnP-(CO2Me) 2] for self-assembly on metal oxide nanoparticles. Efficient and economic synthesis has required a convergent strategy toward reduced symmetry trans-A2B2 and trans-AB2C substitution patterns about the porphyrin macrocycle minimizing the production of porphyrin side products and increasing yields of the target ferrocenylporphyrins. Preliminary spectroscopic data in solution and in the solid state bound to mesoporous TiO2 films are discussed.

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

Alice, Laura Manzoli,Alsimaree, Abdulrahman A.,Frank, Felicity,Hall, Michael John,Knight, Julian Gary,Mauker, Phillip,Penfold, Thomas James,Probert, Michael Richard,Waddell, Paul Gordon

supporting information, (2020/03/25)

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

QUINONE-METHIDE PRECURSORS WITH BODIPY CHROMOPHORE, METHOD OF PREPARATION, BIOLOGICAL ACTIVITY AND APPLICATION IN FLUORESCENT LABELLING

-

Page/Page column 22, (2017/12/15)

The invention relates to BODIPY derivatives of Formula (I) that bear one or more functional groups which in the photochemical reaction upon irradiation with visible light undergo deamination and deliver quinone methides. Furthermore, the invention relates

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