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1-Pyreneisothiocyanate, with the molecular formula C20H10N2S, is an isothiocyanate compound derived from pyrene, a polycyclic aromatic hydrocarbon. This chemical features a sulfur atom bonded to an isothiocyanate group and is renowned for its fluorescent properties. It is widely utilized in chemical research and analysis, particularly for its potential in the development of sensors and probes for detecting specific biomolecules. Due to its fluorescent characteristics, 1-Pyreneisothiocyanate serves as an effective label for proteins and peptides in biochemical and biophysical studies. However, it is crucial to handle 1-PYRENEISOTHIOCYANATE with care, as it may present health and environmental hazards if not managed properly.

24722-90-5

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24722-90-5 Usage

Uses

Used in Chemical Research and Analysis:
1-Pyreneisothiocyanate is used as a research chemical for its fluorescent properties, which facilitate the study and analysis of various chemical compounds and reactions.
Used in Biochemical and Biophysical Studies:
1-Pyreneisothiocyanate is used as a fluorescent label for proteins and peptides, enabling researchers to track and study their behavior and interactions within complex biological systems.
Used in Sensor and Probe Development:
1-Pyreneisothiocyanate is utilized in the development of sensors and probes designed to detect specific biomolecules, thanks to its fluorescent properties that allow for the detection and quantification of target molecules in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 24722-90-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,7,2 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24722-90:
(7*2)+(6*4)+(5*7)+(4*2)+(3*2)+(2*9)+(1*0)=105
105 % 10 = 5
So 24722-90-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H9NS/c19-10-18-15-9-7-13-5-4-11-2-1-3-12-6-8-14(15)17(13)16(11)12/h1-9H

24722-90-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-isothiocyanatopyrene

1.2 Other means of identification

Product number -
Other names 1-Pyreneisothiocyanate

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:24722-90-5 SDS

24722-90-5Relevant academic research and scientific papers

Urea and thiourea based anion receptors in solution and on polymer supports

Byrne,Mullen

, p. 196 - 205 (2018)

Herein we report the development of a new series of surface bound anion sensors exploiting the urea or thiourea motif capable of binding anions through hydrogen bonding interactions. The use of high resolution magic angle spinning 1H NMR allows the direct comparison of the anion binding properties of these receptors in solution versus those tethered to polymer resins. Some intramolecular hydrogen bonding and solvent effects were observed at the solution:surface interface however in general the anion binding properties of the polymer bound urea and thiourea receptors were maintained.

Design and synthesis of preorganized tripodal fluororeceptors based on hydrogen bonding of thiourea groups for optical phosphate ion sensing

Sasaki, Shin-Ichi,Citterio, Daniel,Ozawa, Satoru,Suzuki, Koji

, p. 2309 - 2313 (2007/10/03)

Expecting a preorganization effect, tripodal anion host molecules were designed and synthesized. It was demonstrated that two kinds of new thiourea derivatives having a six-fold substituted benzene ring as a preorganized spacer were effective for recognit

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