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1008498-13-2

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1008498-13-2 Usage

Description

1-(Pyridazin-4-yl)ethanamine is a chemical compound that belongs to the class of organic compounds known as pyridazines and derivatives. Pyridazines are compounds containing a pyridazine ring, which is a six-member aromatic heterocycle, made up of two nitrogen atoms at non-adjacent positions, and four carbon atoms. In the case of 1-(Pyridazin-4-yl)ethanamine, an ethanamine moiety is attached to the pyridazine ring. It is relatively unexplored in the field of chemistry, and not much is known about its specific chemical behavior or potential applications. The exact properties such as melting point, boiling point, and solubility remain unestablished.

Uses

As the specific applications of 1-(Pyridazin-4-yl)ethanamine are not well-documented, it is difficult to provide a comprehensive list of its uses. However, given its chemical structure, it may have potential applications in various industries, such as pharmaceuticals, materials science, or chemical research. Further research and development would be required to explore and confirm its potential uses.
Used in Pharmaceutical Industry:
1-(Pyridazin-4-yl)ethanamine could be used as a chemical intermediate for the synthesis of pharmaceutical compounds, given its unique structure and the presence of the pyridazine ring, which is a common structural motif in many bioactive molecules.
Used in Materials Science:
1-(Pyridazin-4-yl)ethanamine might be used as a building block for the development of new materials with specific properties, such as conductivity, stability, or reactivity, depending on its chemical behavior.
Used in Chemical Research:
1-(Pyridazin-4-yl)ethanamine could serve as a subject of study for chemists to understand its reactivity, stability, and potential interactions with other molecules, which could lead to the discovery of new chemical reactions or processes.

Check Digit Verification of cas no

The CAS Registry Mumber 1008498-13-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,8,4,9 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1008498-13:
(9*1)+(8*0)+(7*0)+(6*8)+(5*4)+(4*9)+(3*8)+(2*1)+(1*3)=142
142 % 10 = 2
So 1008498-13-2 is a valid CAS Registry Number.

1008498-13-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-pyridazin-4-ylethanamine

1.2 Other means of identification

Product number -
Other names methyl-pyridazin-4-ylmethyl-amine

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:1008498-13-2 SDS

1008498-13-2Upstream product

1008498-13-2Downstream Products

1008498-13-2Relevant articles and documents

OXAZOLONE AND PYRROLIDINONE-SUBSTITUTED ARYLAMIDES AS P2X3 AND P2X2/3 ANTAGONISTS

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Page/Page column 24, (2010/12/31)

Compounds of the formula 1: or a pharmaceutically acceptable salt thereof, wherein, X, Y, R1, R2, R3, R4, R5, R6 and R7 are as defined herein. Also disclosed are methods of using the compounds for treating diseases associated with P2X3 and/or a P2X2/3 receptor antagonists and methods of making the compounds.

Preparation of benzindole compounds from naphthalene compounds

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, (2008/06/13)

The invention relates to a process for preparing a substituted 2-amino-benz[cd]indole of the Formula I: STR1 The nitro group of a substituted 1-nitro-8-cyano-naphthalene compound is reduced to an amine group to form a substituted 1-amino-8-cyano-naphthalene compound, which is cyclized to form the substituted 2-amino-benz[cd]indole. The reduction and cyclization may be effected in a one-pot procedure using a reducing agent such as stannous chloride, which generates an acid that cyclizes the reduction product. The syntheses of the 1-nitro-8-cyanonaphthalene compound and its precursors are also described.

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