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11-(9-carbazolyl)undecanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73025-00-0

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73025-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73025-00-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,0,2 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 73025-00:
(7*7)+(6*3)+(5*0)+(4*2)+(3*5)+(2*0)+(1*0)=90
90 % 10 = 0
So 73025-00-0 is a valid CAS Registry Number.
InChI:InChI=1/C23H29NO2/c25-23(26)17-7-5-3-1-2-4-6-12-18-24-21-15-10-8-13-19(21)20-14-9-11-16-22(20)24/h8-11,13-16H,1-7,12,17-18H2,(H,25,26)

73025-00-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-carbazol-9-ylundecanoic acid

1.2 Other means of identification

Product number -
Other names 9-CUA

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:73025-00-0 SDS

73025-00-0Downstream Products

73025-00-0Relevant academic research and scientific papers

Synthesis of Fluorescent Gelators and Direct Observation of Gelation with a Fluorescence Microscope

Hanabusa, Kenji,Ueda, Takuya,Takata, Shingo,Suzuki, Masahiro

, p. 16939 - 16949 (2016)

Fluorescein-, benzothiazole-, quinoline-, stilbene-, and carbazole-containing fluorescent gelators have been synthesized by connecting gelation-driving segments, including l-isoleucine, l-valine, l-phenylalanine, l-leucine residue, cyclo(l-asparaginyl-l-phenylalanyl), and trans-(1R,2R)-diaminocyclohexane. The emission behaviors of the gelators were investigated, and their gelation abilities studied against 15 solvents. The minimum gel concentration, variable-temperature spectroscopy, transmission electron microscopy, scanning electron microscopy, fluorescence microscopy (FM), and confocal laser scanning microscopy (CLSM) were used to characterize gelation. The intermolecular hydrogen bonding between the N?H and C=O of amide, van der Waals interactions and π–π stacking play important roles in gelation. The colors of emission are related to the fluorescence structures of gelators. Fibrous aggregates characterized by the color of their emission were observed by FM. 3D images are produced by the superposition of images captured by CLSM every 0.1 μm to a settled depth. The 3D images show that the large micrometer-sized aggregates spread out three dimensionally. FM observations of mixed gelators are studied. In the case of gelation, two structurally related gelators with the same gelation-driving segment lead to the gelators build up of the same aggregates through similar hydrogen-bonding patterns. When two gelators with structurally different gelation-driving segments induce gelation, the gelators build up each aggregate through individual hydrogen-bonding patterns. A fluorescent reagent that was incorporated into the aggregates of gels through van der Waals interactions was developed. The addition of this fluorescent reagent enables the successful observation of nonfluorescent gelators’ aggregates by FM.

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