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Methanone, (3-amino-6-chloro-4-pyridazinyl)phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145355-23-3

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145355-23-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145355-23-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,3,5 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 145355-23:
(8*1)+(7*4)+(6*5)+(5*3)+(4*5)+(3*5)+(2*2)+(1*3)=123
123 % 10 = 3
So 145355-23-3 is a valid CAS Registry Number.

145355-23-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-amino-6-chloropyridazin-4-yl)-phenylmethanone

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:145355-23-3 SDS

145355-23-3Relevant academic research and scientific papers

RECENT ADVANCES IN PYRIDAZINE CHEMISTRY

Heinisch, Gottfried

, p. 579 - 596 (2007/10/02)

Efficient syntheses of a variety of so far not accessible, monosubstituted or vicinally disubstituted 1,2-diazine derivatives are presented.The versatility of these compounds for syntheses of various polyaza bicyclic and tricyclic systems is demonstrated.

(3-Amino-4-pyridazinyl)phenyl ketones as novel 2-aminobenzophenone isosters: Synthesis and conversion into pyrido[2,3-c]pyridazines. 64th Communication: Syntheses and reactions of pyridazines

Haider,Heinisch,Moshuber

, p. 679 - 682 (2007/10/02)

The preparation of novel diaza analogs of 2-aminobenzophenone (compounds 4, 6) is described. The utility of these bifunctional pyridazine derivatives for the construction of potentially bio-active pyrido[2,3-c]pyridazines is demonstrated.

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