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Acridin-3-ylamine is a chemical compound that belongs to the class of compounds known as acridines, which are polycyclic aromatic compounds containing a three-ring system with two benzene rings joined together by a pyridine ring. It is a slightly acidic, crystalline substance with an amine group that can act as a base and potentially be protonated. Acridin-3-ylamine is commonly found in complex chemical structures, including pharmaceutical drugs, and is known for its characteristics similar to other acridine derivatives.

581-29-3

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581-29-3 Usage

Uses

Used in Pharmaceutical Research:
Acridin-3-ylamine is used as a research compound for investigating its interactions with DNA and its effects on cell apoptosis. Its unique structure and properties make it a promising candidate for the development of new pharmaceutical drugs.
Used in Chemical Research:
Acridin-3-ylamine is used as a chemical research compound to study its properties and potential applications in various fields. Its ability to act as a base and form complexes with other molecules makes it an interesting subject for scientific investigations.
Used in Drug Development:
Acridin-3-ylamine is used as a starting material or intermediate in the synthesis of pharmaceutical drugs. Its presence in complex chemical structures and its potential to interact with biological targets make it a valuable component in drug development processes.

Check Digit Verification of cas no

The CAS Registry Mumber 581-29-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,8 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 581-29:
(5*5)+(4*8)+(3*1)+(2*2)+(1*9)=73
73 % 10 = 3
So 581-29-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H10N2/c14-11-6-5-10-7-9-3-1-2-4-12(9)15-13(10)8-11/h1-8H,14H2

581-29-3SDS

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 acridin-3-amine

1.2 Other means of identification

Product number -
Other names Acridin-3-ylamin

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:581-29-3 SDS

581-29-3Relevant academic research and scientific papers

Application of 2,2,2-trichloroethoxycarbonyl protection to aminoacridines

Zeghida, Walid,Demeunynck, Martine

, p. 231 - 234 (2007)

The 2,2,2-trichloroethoxycarbonyl (Troc) group has been successfully used as a protecting group for aminoacridines. Unlike aliphatic amines, deprotection of these aromatic amines yields significant amounts (12-29%) of stable 2,2-dichloroethoxycarbonyl (Dioc) by-products. Formation of bis-carbamates, through the introduction of butoxycarbonyl (Boc) moieties as temporary protecting groups, efficiently solves this problem. Georg Thieme Verlag Stuttgart.

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