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34246-96-3

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34246-96-3 Usage

Uses

1-methoxypyrene is a pyrene derivative with electroluminescence characteristics. It is used as a reactant in the synthesis of 1-Hydroxypyrene-2-carbaldehyde, a highly selective colorimetric and fluorescent chemosensor for lysine.

Check Digit Verification of cas no

The CAS Registry Mumber 34246-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,4 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34246-96:
(7*3)+(6*4)+(5*2)+(4*4)+(3*6)+(2*9)+(1*6)=113
113 % 10 = 3
So 34246-96-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H12O/c1-18-15-10-8-13-6-5-11-3-2-4-12-7-9-14(15)17(13)16(11)12/h2-10H,1H3

34246-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-METHOXYPYRENE

1.2 Other means of identification

Product number -
Other names Pyrene, 1-methoxy-

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:34246-96-3 SDS

34246-96-3Relevant articles and documents

Stepwise Adsorption of Alkoxy-Pyrene Derivatives onto a Lamellar, Non-Porous Naphthalenediimide-Template on HOPG

Heideman, G. Henrieke,Berrocal, José Augusto,St?hr, Meike,Meijer,Feringa, Ben L.

, p. 207 - 211 (2021)

The development of new strategies for the preparation of multicomponent supramolecular assemblies is a major challenge on the road to complex functional molecular systems. Here we present the use of a non-porous self-assembled monolayer from uC33-NDI-uC33, a naphthalenediimide symmetrically functionalized with unsaturated 33 carbon-atom-chains, to prepare bicomponent supramolecular surface systems with a series of alkoxy-pyrene (PyrOR) derivatives at the liquid/HOPG interface. While previous attempts at directly depositing many of these PyrOR units at the liquid/HOPG interface failed, the multicomponent approach through the uC33-NDI-uC33 template enabled control over molecular interactions and facilitated adsorption. The PyrOR deposition restructured the initial uC33-NDI-uC33 monolayer, causing an expansion in two dimensions to accommodate the guests. As far as we know, this represents the first example of a non-porous or non-metal complex-bearing monolayer that allows the stepwise formation of multicomponent supramolecular architectures on surfaces.

Biotransformation of Pyrene by Cell Cultures of Soybean (Glycine max L.), Wheat (Triticum aestivum L.), Jimsonweed (Datura stramonium L.), and Purple Foxglove (Digitalis purpurea L.)

Hueckelhoven, Ralph,Schuphan, Ingolf,Thiede, Brigitte,Schmidt, Burkhard

, p. 263 - 269 (1997)

The metabolism of the four-ringed polycyclic aromatic hydrocarbon (PAH) pyrene was investigated using cell suspension cultures of soybean, wheat, purple foxglove, and jimsonweed and callus cultures of soybean and foxglove. In all species, nonextractable residues were found (soybean, jimsonweed, and foxglove suspensions, 14C; soybean and foxglove callus cultures, 20-25%; wheat, 30-40%); soluble metabolites were detected in only foxglove and wheat. About 90% of applied pyrene was transformed in wheat. Corresponding data from soybean and foxglove callus cultures were about 30% and those from soybean, jimsonweed, and foxglove suspensions about 7%. In foxglove, 1-hydroxypyrene methyl ether was identified as the main metabolite, whereas a complex mixture of carbohydrate conjugates of 1-hydroxypyrene was found in wheat. Due to the present results, crop and wild plants may be metabolic sinks for PAHs in the environment. Concentrations and toxicological implications of 1-hydroxypyrene, its derivatives, and analogous metabolites of other PAHs should be investigated.

A bispyrene derivative as a selective fluorescent probe for RNA

Liu, Yifan,Jun, Eun Jin,Kim, Gyoungmi,Lee, Ae-Ree,Lee, Joon-Hwa,Yoon, Juyoung

, p. 2505 - 2507 (2014)

A novel bispyrene compound was synthesized to selectively detect RNA through excimer emission "turn-on" in aqueous solution at physiological pH (7.4). The compound was used to successfully image RNA in HeLa cells.

A selective 'Off-On' fluorescent sensor for Zn2+ based on hydrazone-pyrene derivative and its application for imaging of intracellular Zn2+

Zhou, Ying,Kim, Ha Na,Yoon, Juyoung

, p. 125 - 128 (2010)

A simple and effective fluorescent sensor based on hydrazone-pyrene has been synthesized. This probe displays a highly selective fluorescent enhancement with Zn2+, and application of this probe to detect the intrinsic Zn2+ ions present in pancreatic β-cells was successfully demonstrated.

Method for preparing hydroxypyrene compound with high purity

-

, (2021/03/16)

The present invention relates to a method for efficiently removing impurities while minimizing yield loss while minimizing yield loss of a hydroxy pyrene compound as a monomer for manufacturing a polymer compound for a hard mask having anti-reflection characteristics used in a lithographic process of a semiconductor manufacturing process. Pulene purification using pyrene (Pyrene) as starting material The present invention relates to a process for producing a high purity 1 -hydroxypyrene and a process for producing 1 -hydroxypyrene by reacting purified pyrene with a halogen compound under an appropriate solvent and catalyst, and a process for purifying 1 -hydroxypyrene.

Pyrene-like methylthiopyridyl-2-(2- pyro-) Schiff base (Zn Schiff base) base2+ Preparation and application of fluorescent probe

-

Paragraph 0043; 0048-0051, (2019/12/25)

The invention relates to the field of a fluorescence probe, and particularly relates to preparation and application of a pyrenes 2-(2-methylthiopyridine)aniline Schiff base Zn fluorescence probe.The probe has the following concrete structure formula shown in the description. The fluorescence probe can be used for recognizing Zn in a methanol solution. The fluorescence probe has the advantages that the excellent selectivity is shown in other ion competition; higher fluorescence sensing property is realized; the detection limit is low; the sensitivity is high; the fluorescent quantum yield is high.

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