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110999-53-6

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110999-53-6 Usage

Type

Organic compound

Functional Groups

Nitro group, hydroxyethylamine

Class

Pyrazoloacridine compounds

Structure

Contains a dihydropyrazole ring

Biological Activities

Potential pharmaceutical or research applications

Properties

Further analysis and testing required for precise applications

Check Digit Verification of cas no

The CAS Registry Mumber 110999-53-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,9,9 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 110999-53:
(8*1)+(7*1)+(6*0)+(5*9)+(4*9)+(3*9)+(2*5)+(1*3)=136
136 % 10 = 6
So 110999-53-6 is a valid CAS Registry Number.

110999-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dihydro-2-<2-<(2-hydroxyethyl)amino>ethyl>-5-nitropyrazolo<3,4,5-kl>acridin-9-ol

1.2 Other means of identification

Product number -
Other names Pyrazolo(3,4,5-kl)acridin-9-ol,2,6-dihydro-2-(2-((2-hydroxyethyl)amino)ethyl)-5-nitro

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:110999-53-6 SDS

110999-53-6Downstream Products

110999-53-6Relevant articles and documents

2-(Aminoalkyl)-5-nitropyrazoloacridines, a New Class of Anticancer Agents

Capps, David B.,Dunbar, James,Kesten, Suzanne R.,Shillis, Joan,Werbel, Leslie M.,et al.

, p. 4770 - 4778 (2007/10/02)

2-(Aminoalkyl)-5-nitropyrazoloacridines were prepared from substituted anilines via the 1-chloro-4-nitroacridones followed by condensation with hydrazines.Impressive activity was demonstrated for the 9-hydroxy, 9-alkoxy, and 9-acyloxy analogs in vitro on a L1210 leukemia line and in vivo against the P388 leukemia.Advanced studies led to the selection of 3bbb for clinical trial.

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