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CAS

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100241-10-9

1-(6-chloropyridazin-3-yl)piperidin-4-amine(SALTDATA: 2HCl 1.4H2O) is a chemical compound that exists in the form of a dihydrochloride hydrate salt. It is a derivative of piperidine, featuring a chloropyridazine ring, and has potential applications in the pharmaceutical and medicinal fields due to its possible biological activity. The presence of dihydrochloride salt and water molecules in its structure suggests specific solubility and stability properties, which could be crucial for its formulation and use in various applications.

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  • 100241-10-9 Structure

  • Basic information

    1. Product Name: 1-(6-chloropyridazin-3-yl)piperidin-4-amine(SALTDATA: 2HCl 1.4H2O)
    2. Synonyms: 1-(6-chloropyridazin-3-yl)piperidin-4-amine(SALTDATA: 2HCl 1.4H2O);1-(6-chloropyridazin-3-yl)piperidin-4-amine 2HCl
    3. CAS NO:100241-10-9
    4. Molecular Formula: C9H13ClN4
    5. Molecular Weight: 212.67932
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100241-10-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(6-chloropyridazin-3-yl)piperidin-4-amine(SALTDATA: 2HCl 1.4H2O)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(6-chloropyridazin-3-yl)piperidin-4-amine(SALTDATA: 2HCl 1.4H2O)(100241-10-9)
    11. EPA Substance Registry System: 1-(6-chloropyridazin-3-yl)piperidin-4-amine(SALTDATA: 2HCl 1.4H2O)(100241-10-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 100241-10-9(Hazardous Substances Data)

100241-10-9 Usage

Uses

Used in Pharmaceutical Industry:
1-(6-chloropyridazin-3-yl)piperidin-4-amine(SALTDATA: 2HCl 1.4H2O) is used as a potential active pharmaceutical ingredient for the development of new drugs, leveraging its potential biological activity and specific solubility and stability properties.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 1-(6-chloropyridazin-3-yl)piperidin-4-amine(SALTDATA: 2HCl 1.4H2O) serves as a valuable compound for research and development, allowing scientists to explore its properties and investigate its potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 100241-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,2,4 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100241-10:
(8*1)+(7*0)+(6*0)+(5*2)+(4*4)+(3*1)+(2*1)+(1*0)=39
39 % 10 = 9
So 100241-10-9 is a valid CAS Registry Number.

100241-10-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(6-Chloropyridazin-3-yl)piperidin-4-amine

1.2 Other means of identification

Product number -
Other names 1-(6-chloro-3-pyridazinyl)-4-piperidinamine

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:100241-10-9 SDS

100241-10-9Upstream product

100241-10-9Downstream Products

100241-10-9Relevant articles and documents

NEW COMPOUNDS

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Page/Page column 39; 40, (2008/06/13)

The present invention relates to new, potent DPP-IV enzyme inhibitors of the general formula (I), which contain fluorine atoms.

Anti-virally active pyridazinamines

-

, (2008/06/13)

Anti-virally active pyridazinamines, compositions containing the same and methods of treating viral diseases in warm-blooded animals.

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