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2-Amino-4-chloro-6-guanidinopyrimidine is a chemical compound characterized by the molecular formula C5H5ClN6. It presents as a white crystalline powder with a molecular weight of 180.59 g/mol. 2-Amino-4-chloro-6-guanidinopyrimidine is recognized for its potential applications in the pharmaceutical sector, particularly as an intermediate in the synthesis of antiviral and anticancer medications, as well as a building block for guanidine-based compounds. Its exploration for direct antiviral and anticancer properties is also of interest. Due to potential health hazards, it is crucial to handle this chemical with care and adhere to safety protocols.

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  • 83170-03-0 Structure
  • Basic information

    1. Product Name: 2-AMINO-4-CHLORO-6-GUANIDINOPYRIMIDINE
    2. Synonyms: 2-AMINO-4-CHLORO-6-GUANIDINOPYRIMIDINE
    3. CAS NO:83170-03-0
    4. Molecular Formula: C5H7ClN6
    5. Molecular Weight: 186.6
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83170-03-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 424.132 °C at 760 mmHg
    3. Flash Point: 210.308 °C
    4. Appearance: /
    5. Density: 1.899 g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.814
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-AMINO-4-CHLORO-6-GUANIDINOPYRIMIDINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-AMINO-4-CHLORO-6-GUANIDINOPYRIMIDINE(83170-03-0)
    12. EPA Substance Registry System: 2-AMINO-4-CHLORO-6-GUANIDINOPYRIMIDINE(83170-03-0)
  • 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: 83170-03-0(Hazardous Substances Data)

83170-03-0 Usage

Uses

Used in Pharmaceutical Industry:
2-Amino-4-chloro-6-guanidinopyrimidine serves as a crucial intermediate in the synthesis of various drugs, specifically those with antiviral and anticancer properties. Its role in drug development is pivotal, contributing to the creation of life-saving medications.
Used in the Synthesis of Guanidine-based Compounds:
As a building block, 2-Amino-4-chloro-6-guanidinopyrimidine is instrumental in the production of guanidine-based compounds, which have a wide range of applications in chemical and pharmaceutical processes.
Used in Antiviral and Anticancer Research:
2-Amino-4-chloro-6-guanidinopyrimidine is under investigation for its intrinsic antiviral and anticancer properties, which could lead to the development of new therapeutic agents for the treatment of viral infections and cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 83170-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,1,7 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83170-03:
(7*8)+(6*3)+(5*1)+(4*7)+(3*0)+(2*0)+(1*3)=110
110 % 10 = 0
So 83170-03-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H7ClN6/c6-2-1-3(11-4(7)8)12-5(9)10-2/h1H,(H6,7,8,9,10,11,12)

83170-03-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-amino-6-chloropyrimidin-4-yl)guanidine

1.2 Other means of identification

Product number -
Other names 2-AMINO-4-CHLORO-6-GUANIDINOPYRIMIDINE

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:83170-03-0 SDS

83170-03-0Relevant articles and documents

Coordination Compounds of Copper(II) with Aminoguanidinopyrimidines

Zawadzki, H. J.

, p. 1293 - 1302 (2007/10/02)

Some new chelates of copper(II) with substituted guanidinopyrimidines have been obtained and characterized. On the basis of IR and VIS spectra the structure of the nearest environment of the central ion in these chelates has been determined. These ligands are bonded with metal ion via the nitrogens atoms of pyrimidine heterocyclic ring and guanidine group. Key words: complexes, synthesis, IR-spectra

Synthesis of Some Substituted Guanidinopyrimidines and their Structural Assignment by 13C and 1H NMR

Ladd, David L.

, p. 917 - 921 (2007/10/02)

A series of substituted 2- and 4-guanidinopyrimidines were prepared by reaction of halopyrimidines with guanidine; alkylamino and amino substituents were introduced by subsequent halogen replacement by primary amines or ammonia or the catalytic reduction of nitro groups.Structural assignments were made on the basis of 13C and 1H nmr.A guanidinopteridine and a bispyrimidinylguanidine were also synthesized.Some unsuccessful reaction illustrated the low nucleophilic reactivity and thermal instability of the guanidine group.

Guanidinopyrimidine compounds, compositions and method of using as a diuretic

-

, (2008/06/13)

2,4-Amino, guanidinopyrimidines have diuretic activity. A representative species of these compounds is 2-guanidino-4-amino-6-chloroguanidine which is prepared by the stepwise replacement of first the 2-halo of a 2,4,6-trihalopyrimidine by guanidino and then the 4-halo by ammonia.

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