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5-Chloro-1-Methyl-1H-pyrazol-3-aMine, also known as CM-pyrazole, is a chemical compound with the formula C4H6ClN3. It is a derivative of pyrazole and is commonly used as a building block in organic synthesis for the production of pharmaceuticals, agrochemicals, and other fine chemicals. This versatile compound exhibits antimicrobial, antiviral, and anticancer activities, making it a valuable tool in drug discovery and development. Additionally, it is used in the synthesis of various heterocyclic compounds, establishing its importance as an intermediate in the chemical industry.

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  • 1191453-81-2 Structure
  • Basic information

    1. Product Name: 5-Chloro-1-Methyl-1H-pyrazol-3-aMine
    2. Synonyms: 5-Chloro-1-Methyl-1H-pyrazol-3-aMine
    3. CAS NO:1191453-81-2
    4. Molecular Formula: C4H6ClN3
    5. Molecular Weight: 131.56354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1191453-81-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 268.0±20.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.48±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    8. Solubility: N/A
    9. PKA: 2.99±0.11(Predicted)
    10. CAS DataBase Reference: 5-Chloro-1-Methyl-1H-pyrazol-3-aMine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-Chloro-1-Methyl-1H-pyrazol-3-aMine(1191453-81-2)
    12. EPA Substance Registry System: 5-Chloro-1-Methyl-1H-pyrazol-3-aMine(1191453-81-2)
  • 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: 1191453-81-2(Hazardous Substances Data)

1191453-81-2 Usage

Uses

Used in Pharmaceutical Industry:
5-Chloro-1-Methyl-1H-pyrazol-3-aMine is used as a building block for the synthesis of pharmaceuticals due to its antimicrobial, antiviral, and anticancer properties. It contributes to the development of new drugs that target a wide range of diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical industry, 5-Chloro-1-Methyl-1H-pyrazol-3-aMine is used as a key intermediate for the production of agrochemicals. Its antimicrobial properties make it suitable for the development of pesticides and other agricultural chemicals that protect crops from diseases and pests.
Used in Fine Chemicals Industry:
5-Chloro-1-Methyl-1H-pyrazol-3-aMine is utilized as a building block in the synthesis of various fine chemicals. Its versatility allows for the creation of specialty chemicals used in a wide range of applications, from fragrances to dyes.
Used in Heterocyclic Compounds Synthesis:
5-Chloro-1-Methyl-1H-pyrazol-3-aMine is used as an important intermediate in the synthesis of heterocyclic compounds. Its unique structure and reactivity make it a valuable component in the creation of complex organic molecules with diverse applications in various industries.
Used in Research and Development:
Across various scientific disciplines, 5-Chloro-1-Methyl-1H-pyrazol-3-aMine is used in research and development. Its diverse applications and potential for new discoveries make it an essential tool for scientists working in fields such as medicinal chemistry, materials science, and chemical engineering.

Check Digit Verification of cas no

The CAS Registry Mumber 1191453-81-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,1,4,5 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1191453-81:
(9*1)+(8*1)+(7*9)+(6*1)+(5*4)+(4*5)+(3*3)+(2*8)+(1*1)=152
152 % 10 = 2
So 1191453-81-2 is a valid CAS Registry Number.

1191453-81-2SDS

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 5-chloro-1-methylpyrazol-3-amine

1.2 Other means of identification

Product number -
Other names 5-chloro-1-methyl-1H-pyrazol-3-ylamine

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:1191453-81-2 SDS

1191453-81-2Downstream Products

1191453-81-2Relevant articles and documents

SUBSTITUTED PYRIMIDINE COMPOUNDS, COMPOSITIONS AND MEDICINAL APPLICATIONS THEREOF

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Paragraph 000153, (2015/03/13)

The present disclosure relates to pyrimidine compounds of formula (I), their stereoisomers, tautomers, pharmaceutically acceptable salts, polymorphs, solvates, and hydrates thereof. The present disclosure also relates to process of preparation of these pyrimidine compounds, and to pharmaceutical compositions containing them. The compounds of the present disclosure are useful in the treatment, prevention or suppression of diseases and disorders mediated by epidermal growth factor receptor (EGFR) family kinases.

PYRIDAZINONE GLUCOKINASE ACTIVATORS

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Page/Page column 43, (2009/10/30)

Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of metabolic diseases and disorders such as, for example, type II diabetes mellitus.

8-substituted pyrazolopentathiepins and related compounds

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, (2008/06/13)

Heteropentathiepins including pyrazolopentathiepins substituted in the 8-position; intermediate pyrazolo-1,2,3-thiadiazoles, pyrazolothiazathiolium chlorides, and 5-substituted aminopyrazoles; process for making the pentathiepins by reacting the corresponding 1,2,3-thiadiazoles with sulfur at elevated temperatures; process for making the thiazathiolium chlorides; and use of the pentathiepins as fungicides or as sulfur sensitizers in photographic emulsions.

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