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2-bromo-3-hydroxy-2,3-dimethyl-1,2,3,4-tetrahydrobenzo[g]pyridazino[1,2-b]phthalazine-6,13-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65417-04-1

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65417-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65417-04-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,1 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65417-04:
(7*6)+(6*5)+(5*4)+(4*1)+(3*7)+(2*0)+(1*4)=121
121 % 10 = 1
So 65417-04-1 is a valid CAS Registry Number.

65417-04-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-3-hydroxy-2,3-dimethyl-1,2,3,4-tetrahydro-benzo[g]pyridazino[1,2-b]phthalazine-6,13-dione

1.2 Other means of identification

Product number -
Other names -

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:65417-04-1 SDS

65417-04-1Downstream Products

65417-04-1Relevant academic research and scientific papers

The steric course of some electrophilic additions to the tetrahydropyridazine ring moiety of benzo[g]phthalazino[1,2-b]pyridazine-6,13-dione derivatives. I.

Cano,Gomez-Contreras,Sanz,Yunta

, p. 243 - 254 (1993)

The functionalization of ring A in diazatetracyclic analogues of anthracyclinones via electrophilic addition of psotive halogen sources has been investigated. Bromine azide, iodine azide, NBS/H2O/DMSO and NBS/EtOH were the reactions of choice. Dehydrohalogenation and further regiospecific addition products to the C-1/C-2 double bond have been found in most cases besides the expected addition compounds. Conformational homogeneity and trans-axial orientations are shown by all the isolated compounds. The influence of the attacking species over the nuycleophilic step and that of the carbonyl neighbouring group over the conformational features have been evaluated.

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