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5-Amino-2,4,6-trichloropyrimidine is a chemical compound with the molecular formula C4HCl3N4. It is a derivative of pyrimidine and contains three chlorine atoms and an amino group. 5-Amino-2,4,6-trichloropyrimidine is known for its versatile reactivity and biological activity, making it a valuable intermediate in chemical synthesis.

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  • 91322-00-8 Structure
  • Basic information

    1. Product Name: 5-Amino-2,4,6-trichloropyrimidine
    2. Synonyms: 5-Amino-2,4,6-trichloropyrimidine;2,4,6-Trichloro-5-pyrimidinamine;2,4,6-Trichloro-pyrimidin-5-ylamine;2,4,6-TRICHLOROPYRIMIDIN-5-AMINE(WXC08712)
    3. CAS NO:91322-00-8
    4. Molecular Formula: C4H2Cl3N3
    5. Molecular Weight: 198.43778
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 91322-00-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 260℃
    3. Flash Point: 111℃
    4. Appearance: /
    5. Density: 1.740
    6. Vapor Pressure: 0.013mmHg at 25°C
    7. Refractive Index: 1.645
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: -3.97±0.10(Predicted)
    11. CAS DataBase Reference: 5-Amino-2,4,6-trichloropyrimidine(CAS DataBase Reference)
    12. NIST Chemistry Reference: 5-Amino-2,4,6-trichloropyrimidine(91322-00-8)
    13. EPA Substance Registry System: 5-Amino-2,4,6-trichloropyrimidine(91322-00-8)
  • 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: 91322-00-8(Hazardous Substances Data)

91322-00-8 Usage

Uses

Used in Pharmaceutical Synthesis:
5-Amino-2,4,6-trichloropyrimidine is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications in medicine.
Used in Agrochemical Production:
In the agrochemical industry, 5-Amino-2,4,6-trichloropyrimidine serves as a building block for the creation of effective pesticides and other crop protection agents. Its incorporation into these products enhances their pesticidal properties, contributing to improved agricultural yields.
Used in Organic Compounds Production:
5-Amino-2,4,6-trichloropyrimidine is utilized as a versatile starting material in the production of a wide range of organic compounds. Its reactivity and functional groups enable the synthesis of various organic molecules with diverse applications in different industries.
Used in Material Science:
In the field of material science, 5-Amino-2,4,6-trichloropyrimidine has potential applications in the development of new materials with unique properties. Its incorporation into these materials can lead to advancements in areas such as polymer science, nanotechnology, and other emerging fields.
Overall, 5-Amino-2,4,6-trichloropyrimidine is a multifaceted chemical compound with a broad range of applications across various industries, including pharmaceuticals, agrochemicals, organic compounds production, and material science. Its unique structure and reactivity make it an essential intermediate in chemical synthesis and a promising candidate for the development of innovative products and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 91322-00-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,2 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91322-00:
(7*9)+(6*1)+(5*3)+(4*2)+(3*2)+(2*0)+(1*0)=98
98 % 10 = 8
So 91322-00-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H2Cl3N3/c5-2-1(8)3(6)10-4(7)9-2/h8H2

91322-00-8SDS

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 2,4,6-trichloropyrimidin-5-amine

1.2 Other means of identification

Product number -
Other names 2,4,6-Trichlor-pyrimidin-5-ylamin

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:91322-00-8 SDS

91322-00-8Relevant articles and documents

Synthesis of ticagrelor analogues belonging to 1,2,3-triazolo[4,5-d]pyrimidines and study of their antiplatelet and antibacterial activity

Goffin, Eric,Jacques, Nicolas,Lancellotti, Patrizio,Musumeci, Lucia,Nchimi, Alain,Pirotte, Bernard,Oury, Cécile

, (2020/09/11)

Based on the recent observation that the antiplatelet agent ticagrelor and one of its metabolite exert bactericidal activity against gram-positive bacteria, a series of 1,2,3-triazolo[4,5-d]pyrimidines structurally related to ticagrelor were synthesized and examined as putative antiplatelet and antibacterial agents. The aim was to assess the possibility of dissociating the two biological properties and to find novel 1,2,3-triazolo[4,5-d]pyrimidines expressing antiplatelet activity and devoid of in vitro antibacterial activity. The new compounds synthesized were known metabolites of ticagrelor as well as structurally simplified analogues. Some of them were found to express antiplatelet activity and to lose the antibacterial activity, supporting the view that the two activities were not necessarily linked.

FERROPORTIN INHIBITORS AND METHODS OF USE

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Paragraph 0393; 0394, (2020/07/07)

The subject matter described herein is directed to Ferroportin inhibitor compounds of Formula I and pharmaceutical salts thereof, methods of preparing the compounds, pharmaceutical compositions comprising the compounds and methods of administering the compounds for prophylaxis and/or treatment of diseases caused by a lack of hepcidin or iron metabolism disorders, particularly iron overload states, such as thalassemia, sickle cell disease and hemochromatosis.

HEXAHYDROOXAZINOPTERINE COMPOUNDS

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Page/Page column 13, (2011/04/14)

The present invention provides mTOR inhibitors of the formula wherein the variables are as defined herein. Also provided are pharmaceutical compositions, kits and articles of manufacture comprising such compounds; methods of making the compounds and intermediates thereof; and methods of using the compounds.

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