Welcome to LookChem.com Sign In|Join Free

CAS

  • or

53761-46-9

Post Buying Request

53761-46-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

53761-46-9 Usage

Type of compound

Dye

Usage

Medical and biological research

Function

Fluorescent marker for protein aggregation and fibril formation

Specific application

Studies related to Alzheimer's disease and other neurodegenerative disorders

Affinity

High affinity for amyloid fibrils

Binding property

Emits a strong fluorescent signal when bound to amyloid structures

Utility

Visualization and quantification of protein aggregates

Research focus

Understanding the mechanisms of amyloid formation

Relevance

Development of potential therapeutics for amyloid-related diseases

Check Digit Verification of cas no

The CAS Registry Mumber 53761-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,6 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53761-46:
(7*5)+(6*3)+(5*7)+(4*6)+(3*1)+(2*4)+(1*6)=129
129 % 10 = 9
So 53761-46-9 is a valid CAS Registry Number.

53761-46-9SDS

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 1,4,7-trimethylquinolin-2-one

1.2 Other means of identification

Product number -
Other names 1,4,7-trimethylquinolin-2(1h)-one

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:53761-46-9 SDS

53761-46-9Relevant articles and documents

Ru-NHC-Catalyzed Asymmetric Hydrogenation of 2-Quinolones to Chiral 3,4-Dihydro-2-Quinolones

Daniliuc, Constantin,Glorius, Frank,Hu, Tianjiao,Lückemeier, Lukas

, p. 23193 - 23196 (2021/09/25)

Direct enantioselective hydrogenation of unsaturated compounds to generate chiral three-dimensional motifs is one of the most straightforward and important approaches in synthetic chemistry. We realized the Ru(II)-NHC-catalyzed asymmetric hydrogenation of 2-quinolones under mild reaction conditions. Alkyl-, aryl- and halogen-substituted optically active dihydro-2-quinolones were obtained in high yields with moderate to excellent enantioselectivities. The reaction provides an efficient and atom-economic pathway to construct simple chiral 3,4-dihydro-2-quinolones. The desired products could be further reduced to tetrahydroquinolines and octahydroquinolones.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 53761-46-9