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75535-22-7

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75535-22-7 Usage

Type of compound

Carbonyl compound

Structure

Contains a quinoline ring structure with a six-carbon chain attached

Usage

Building block for organic synthesis and pharmaceutical research, component of fragrance and flavor formulations

Biological activities

Potential as an inhibitor of certain enzymes

Industrial and scientific applications

Of interest due to its chemical structure and properties

Check Digit Verification of cas no

The CAS Registry Mumber 75535-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,5,3 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 75535-22:
(7*7)+(6*5)+(5*5)+(4*3)+(3*5)+(2*2)+(1*2)=137
137 % 10 = 7
So 75535-22-7 is a valid CAS Registry Number.

75535-22-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Ethyl-1,2,3,4-tetrahydro-6-Quinolinecarboxaldehyde

1.2 Other means of identification

Product number -
Other names 1-Ethyl-1,2,3,4,6,7-hexahydroindolo(2,3-a)quinolizinium

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:75535-22-7 SDS

75535-22-7Downstream Products

75535-22-7Relevant articles and documents

Novel aza-BODIPY based small molecular NIR-II fluorophores for: In vivo imaging

Bai, Lei,Sun, Pengfei,Liu, Yi,Zhang, Hang,Hu, Wenbo,Zhang, Wansu,Liu, Zhipeng,Fan, Quli,Li, Lin,Huang, Wei

supporting information, p. 10920 - 10923 (2019/09/18)

The development of new NIR-II fluorophores, particularly those with facile syntheses, high fluorescence quantum yields, and stable and tunable photophysical properties, is challenging. Herein, we report a new class of small molecular NIR-II fluorophores based on aza-dipyrromethene boron difluoride (aza-BODIPY) dyes. We demonstrate promising photophysical properties of these dyes, such as large Stokes shift, superior photostability, and good fluorescence brightness as nanoparticles in aqueous solution. Because of these properties and high resolution and deep penetration NIR-II imaging ability, the aza-BODIPY based dyes show great potential as NIR-II imaging agents.

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