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6-chloro-N-(propan-2-yl)pyridazin-3-amine is a chemical compound with a molecular formula of C7H10ClN3. It belongs to the class of organic compounds known as pyridazines and pyridazine derivatives, which are characterized by a six-membered aromatic ring with two nitrogen atoms at positions 1 and 2, and four carbon atoms. This specific compound is distinguished by the presence of a propan-2-yl group attached to the nitrogen atom and a chlorine atom at the 6th carbon of the pyridazine ring. While its physical and chemical properties, as well as toxicological data, are not extensively documented in scientific literature, its potential applications in various industries could be significant.

1007-55-2

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1007-55-2 Usage

Uses

Given the limited information available on 6-chloro-N-(propan-2-yl)pyridazin-3-amine, its uses can only be speculated based on the general properties of pyridazine derivatives. However, it is important to note that without specific data, the following applications are hypothetical and would require further research and validation.
Used in Pharmaceutical Industry:
6-chloro-N-(propan-2-yl)pyridazin-3-amine could be used as an intermediate in the synthesis of pharmaceutical compounds, given the structural features that may allow for the formation of various bioactive molecules. Its potential role in drug development could be for the treatment of a range of diseases, depending on the specific properties and reactivity of the compound.
Used in Chemical Research:
In the field of chemical research, 6-chloro-N-(propan-2-yl)pyridazin-3-amine might serve as a model compound for studying the reactivity and properties of pyridazine derivatives. This could lead to a better understanding of the chemical behavior of similar compounds and contribute to the development of new synthetic methods or applications.
Used in Material Science:
6-chloro-N-(propan-2-yl)pyridazin-3-amine could potentially be explored for its properties in material science, such as its potential use in the development of new materials with specific electronic, optical, or mechanical properties. The presence of the chlorine atom and the propan-2-yl group might influence its ability to form complexes or participate in reactions that could be useful in material synthesis.
It is crucial to emphasize that these applications are speculative and would require extensive research, including synthesis, characterization, and testing, to determine the true potential of 6-chloro-N-(propan-2-yl)pyridazin-3-amine in these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1007-55-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1007-55:
(6*1)+(5*0)+(4*0)+(3*7)+(2*5)+(1*5)=42
42 % 10 = 2
So 1007-55-2 is a valid CAS Registry Number.

1007-55-2SDS

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 6-chloro-N-propan-2-ylpyridazin-3-amine

1.2 Other means of identification

Product number -
Other names 3-Chlor-6-isopropylamino-pyridazin

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:1007-55-2 SDS

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1007-55-2Relevant academic research and scientific papers

Quinoxaline studies. 23. Potential antimalarials. Substituted 5,8-dimethoxy-6-[N-(omega-dimethylaminoalkyl)amino]quinoxalines were prepared: the first series with identical 2,3-substituents H, CH3, C6H5, C6H4-4-Cl, and CH2C6H5; and the second with identical styryl groups CH=CHC6H5, CH=CHC6H4-4-Cl, CH=CHC6H3-3,4-Cl2, CH=CHC6H4-4-F, CH=CHC6H4-4-CF3, and CH=CHC6H4-4-NO2. None of the substances

Pifferi,Parravicini,Carpi,Dorigotti

, p. 741 - 746 (2007/10/04)

3-Hydrazinopyridazines substituted in position 6 with a primary amine, secondary amine, or an alkoxy group were synthesized and screened for antihypertensive activity. In general, the 6-dialklamino derivatives are the most active; the (2-hydroxypropyl)methylamino chain provides the best combination of high antihypertensive activity and toxicity.

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