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N-acridin-9-ylglycine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55468-69-4

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55468-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55468-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,6 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55468-69:
(7*5)+(6*5)+(5*4)+(4*6)+(3*8)+(2*6)+(1*9)=154
154 % 10 = 4
So 55468-69-4 is a valid CAS Registry Number.

55468-69-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(acridin-9-ylamino)acetic acid

1.2 Other means of identification

Product number -
Other names Glycine,N-9-acridinyl

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:55468-69-4 SDS

55468-69-4Downstream Products

55468-69-4Relevant academic research and scientific papers

9-AMINOACRIDINE DERIVATIVES, THEIR PREPARATION AND USES

-

Page/Page column 26-27, (2011/05/11)

N-substituted 9-aminoacridine and bis-acridino derivatives containing electron- withdrawing groups (EWG) or electron-donating groups (EDG), including amino acid residues, and one-pot methods for their synthesis are disclosed. The derivatives are potential

One-pot derivatization of medicinally important 9-aminoacridines by reductive amination and SNAr reaction

Gellerman, Gary,Gaisin, Vladimir,Brider, Tamara

experimental part, p. 836 - 839 (2010/03/04)

A new highly efficient one-pot derivatization of medicinally important 9-aminoacridines (9-AA) at the amine position is described. Simple reductive amination and SNAr reaction using easily accessible starting materials give a fast entry to novel 9-AA derivatives for biological screening.

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