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ETHYL 5-AMINO-1-(3-NITROPHENYL)PYRAZOLE-4-CARBOXYLATE is a pyrazole derivative with the molecular formula C12H11N5O4. It is characterized by the presence of an ethyl ester group, an amino group, and a nitrophenyl group. This chemical compound may hold potential in the fields of organic synthesis and medicinal chemistry due to its unique structure and functional groups. Further research and testing are required to determine its specific properties and potential applications.

16459-34-0

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16459-34-0 Usage

Uses

Used in Organic Synthesis:
ETHYL 5-AMINO-1-(3-NITROPHENYL)PYRAZOLE-4-CARBOXYLATE is used as a building block or intermediate in organic synthesis for the development of new compounds with various applications. Its functional groups, such as the ethyl ester and amino group, can be utilized in chemical reactions to form a wide range of products.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, ETHYL 5-AMINO-1-(3-NITROPHENYL)PYRAZOLE-4-CARBOXYLATE is used as a potential candidate for the development of new pharmaceuticals. Its unique structure and functional groups may contribute to the design of novel drugs with specific therapeutic properties. Further research is needed to explore its potential as a lead compound in drug discovery and development.
Used in Chemical Research:
ETHYL 5-AMINO-1-(3-NITROPHENYL)PYRAZOLE-4-CARBOXYLATE is also used in chemical research to study the properties and reactivity of pyrazole derivatives. Its structure and functional groups provide a basis for understanding the behavior of similar compounds and can contribute to the advancement of chemical knowledge in this area.
Used in Analytical Chemistry:
In analytical chemistry, ETHYL 5-AMINO-1-(3-NITROPHENYL)PYRAZOLE-4-CARBOXYLATE can be employed as a reference compound or standard for the development and validation of analytical methods. Its unique structure and properties can be used to evaluate the performance of various analytical techniques, such as chromatography, spectroscopy, and mass spectrometry.
Used in Material Science:
ETHYL 5-AMINO-1-(3-NITROPHENYL)PYRAZOLE-4-CARBOXYLATE may also find applications in material science, where its unique structure and functional groups can be utilized to develop new materials with specific properties. For example, it could be used in the synthesis of polymers, coatings, or other materials with tailored characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 16459-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,5 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16459-34:
(7*1)+(6*6)+(5*4)+(4*5)+(3*9)+(2*3)+(1*4)=120
120 % 10 = 0
So 16459-34-0 is a valid CAS Registry Number.

16459-34-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 5-AMINO-1-(3-NITROPHENYL)PYRAZOLE-4-CARBOXYLATE

1.2 Other means of identification

Product number -
Other names M-1415

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:16459-34-0 SDS

16459-34-0Relevant articles and documents

AZOLOPYRIMIDINES AS INHIBITORS OF CANNABINOID 1 ACTIVITY

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Page/Page column 63, (2008/06/13)

The invention provides compounds of formula (Ia), (Ic), (Ig) and (Ik), pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with the activity of Cannabinoid Receptor 1 (CB1).

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