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4-Amino-2-chloro-1,3,5-triazine is an organic compound with the chemical formula C2H3ClN4. It is a derivative of the triazine family, characterized by its three nitrogen atoms forming a ring structure. This particular compound has a chlorine atom attached to the 2nd carbon and an amino group on the 4th carbon. It is a white crystalline solid and is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and dyes. Due to its reactivity, it is important to handle this compound with care, as it can be toxic and may have potential environmental impacts.

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  • 7709-13-9 Structure
  • Basic information

    1. Product Name: 4-AMino-2-chloro-1,3,5-triazine
    2. Synonyms: 4-AMino-2-chloro-1,3,5-triazine;4-chloro-1,3,5-triazin-2-amine
    3. CAS NO:7709-13-9
    4. Molecular Formula: C3H3ClN4
    5. Molecular Weight: 130.53572
    6. EINECS: N/A
    7. Product Categories: Amines;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;Amines, Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals
    8. Mol File: 7709-13-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 383.3°C at 760 mmHg
    3. Flash Point: 185.6°C
    4. Appearance: /
    5. Density: 1.566g/cm3
    6. Vapor Pressure: 4.45E-06mmHg at 25°C
    7. Refractive Index: 1.63
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    9. Solubility: Dichloromethane, Methanol
    10. PKA: 2.62±0.10(Predicted)
    11. CAS DataBase Reference: 4-AMino-2-chloro-1,3,5-triazine(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-AMino-2-chloro-1,3,5-triazine(7709-13-9)
    13. EPA Substance Registry System: 4-AMino-2-chloro-1,3,5-triazine(7709-13-9)
  • 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: 7709-13-9(Hazardous Substances Data)

7709-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7709-13-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,0 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7709-13:
(6*7)+(5*7)+(4*0)+(3*9)+(2*1)+(1*3)=109
109 % 10 = 9
So 7709-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C3H3ClN4/c4-2-6-1-7-3(5)8-2/h1H,(H2,5,6,7,8)

7709-13-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-1,3,5-triazin-2-amine

1.2 Other means of identification

Product number -
Other names 4-Amino-2-chloro-1,3,5-triazine

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:7709-13-9 SDS

7709-13-9Relevant articles and documents

SUBSTITUTED (PIPERIDIN-1-YL)ARYL ANALOGUES FOR MODULATING AVILACTIVITY

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Paragraph 0364-0366, (2020/11/12)

In one aspect, the disclosure relates to compounds useful to regulate, limit, or inhibit the expression of AVIL (advillin), methods of making same, pharmaceutical compositions comprising same, and methods of treating disorders associated with AVIL dysregulation using same. In aspects, the disclosed compounds, compositions and methods are useful for treating disorders or diseases in which the regulation, limitation, or inhibition of the expression of AVIL can be clinically useful, such as, for example, the treatment of cancer. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present disclosure.

INHIBITORS OF CELLULAR METABOLIC PROCESSES

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Page/Page column 180, (2018/03/25)

The invention provides inhibitor compounds of MAT2A that are useful as therapeutic agents for treating malignancies wherein the compounds have the general formula (I) : wherein ring A, ring B, ring C and, R1 are as described herein.

NOVEL HETEROARYL AND HETEROCYCLE COMPOUNDS, COMPOSITIONS AND METHODS

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Page/Page column 126; 127, (2014/02/16)

The invention relates to novel heteroaryl and heterocycle compounds and pharmaceutical compositions comprising them, uses and methods thereof for inhibiting the activity of PI3k and for treating inflammatory and autoimmune disorders diseases and cancer.

NOVEL HETEROARYL AND HETEROCYCLE COMPOUNDS, COMPOSITION AND METHODS THEREOF

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Page/Page column 151, (2014/02/16)

Disclosed are novel heteroaryl and heterocycle compounds of formula I-1, I-2 or I-3 and pharmaceutical compositions comprising them, uses and methods thereof for inhibiting the activity of PI3K and for treating inflammatory and autoimmune diseases and cancer.

NOVEL HETEROARYL AND HETEROCYCLE COMPOUNDS, COMPOSITIONS AND METHODS

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Page/Page column 151; 152, (2014/02/16)

Provided are novel heteroaryl and heterocycle compounds of formula (I-1), (I-2) or (I-3) and pharmaceutical compositions comprising them, uses and methods thereof for inhibiting the activity of PI3K and for treating inflammatory and autoimmune disorders diseases and cancer.

CHEMICAL COMPOUNDS, COMPOSITIONS AND METHODS FOR KINASE MODULATION

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Page/Page column 108, (2011/12/04)

Chemical compounds that modulate kinase activity, including PI3 kinase activity, and chemical compounds, pharmaceutical compositions, and methods of treatment of diseases and conditions associated with kinase activity, including PI3 kinase activity, are described herein.

4-Amino-2-chloro-1,3,5-triazine: A New Metabolite of Atrazine by a Soil Bacterium

Giardina, M. C.,Giardi, M. T.,Filacchioni, G.

, p. 2067 - 2072 (2007/10/02)

The degradation of herbicide atrazine (2-chloro-4-ethylamino-6-isopropylamino-1,3,5-triazine) by a soil bacterium is reported.The bacterium involved is a species of Nocardia, which utilizes the atrazine as the sole source of carbon and nitrogen.A new metabolite, 4-amino-2-chloro-1,3,5-triazine, of the degradation of atrazine in the presence of glucose has been identified.The results further substantiated that atrazine can be degraded by soil microorganisms and indicated that deamination can also occur, as well as dealkylation. 4-Amino-2-chloro-1,3,5-triazine did not show phytotoxic activity to oat (Avena sativa L.), demonstrating that deamination insures detoxification.

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