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135659-91-5

1,2,3-Triazine-5-carboxamide,4,6-dimethyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 135659-91-5 Structure

  • Basic information

    1. Product Name: 1,2,3-Triazine-5-carboxamide,4,6-dimethyl-(9CI)
    2. Synonyms: 1,2,3-Triazine-5-carboxamide,4,6-dimethyl-(9CI)
    3. CAS NO:135659-91-5
    4. Molecular Formula: C6H8N4O
    5. Molecular Weight: 152.15392
    6. EINECS: N/A
    7. Product Categories: AMIDE
    8. Mol File: 135659-91-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 299.7±50.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.264±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 12.65±0.50(Predicted)
    10. CAS DataBase Reference: 1,2,3-Triazine-5-carboxamide,4,6-dimethyl-(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,2,3-Triazine-5-carboxamide,4,6-dimethyl-(9CI)(135659-91-5)
    12. EPA Substance Registry System: 1,2,3-Triazine-5-carboxamide,4,6-dimethyl-(9CI)(135659-91-5)

  • 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: 135659-91-5(Hazardous Substances Data)

135659-91-5 Usage

Appearance

White to light yellow crystalline powder

Chemical Class

Amide derivative of 1,2,3-triazine

Potential Applications

a. Pharmaceuticals
b. Agriculture
c. Materials Science

Usage

a. Synthesis of other organic compounds
b. Exhibiting biological activities

Importance

Valuable building block for drug discovery and development

Research Status

Further research needed to fully understand its properties and potential uses

Check Digit Verification of cas no

The CAS Registry Mumber 135659-91-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,6,5 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 135659-91:
(8*1)+(7*3)+(6*5)+(5*6)+(4*5)+(3*9)+(2*9)+(1*1)=155
155 % 10 = 5
So 135659-91-5 is a valid CAS Registry Number.

135659-91-5SDS

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 4,6-Dimethyl-1,2,3-triazine-5-carboxamide

1.2 Other means of identification

Product number -
Other names 3H-Azepine-5-carboxamide,2-(1-piperidinyl)

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:135659-91-5 SDS

135659-91-5Downstream Products

135659-91-5Relevant articles and documents

RADICAL NUCLEOPHILIC CARBAMOYLATION OF 1,2,3-TRIAZINE DERIVATIVES

Nagata, Kazuhiro,Itoh, Takashi,Okada, Mamiko,Takahashi, Hiroyuki,Ohsawa, Akio

, p. 2015 - 2022 (2007/10/02)

Radical nucleophilic carbamoylation was carried out to various 1,2,3-triazine derivatives.In the case of parent triazines as substrates, Minisci's system was not effective, and in the absence of acid, a small ammount of radical adduct was obtained.Triazinium dicyanomethylides reacted with carbamoyl radical to give 5- carbamoyl triazines in good yields.Other 1,2,3-triazine derivatives were also investigated.

RADICAL CARBAMOYLATION OF 1,2,3-TRIAZINIUM 2-DICYANOMETHYLIDES

Nagata, Kazuhiro,Itoh, Takashi,Okada, Mamiko,Takahashi, Hiroyuki,Ohsawa, Akio

, p. 855 - 857 (2007/10/02)

The nucleophilic radical carbamoylation of 4,6-disubstituted 1,2,3-triazinium 2-dicyanomethylides occurred at their 5-positions followed by the elimination of dicyanomethylene to form 5-substituted 1,2,3-triazines.The reaction did not proceed when parent triazines were adopted as the substrates.

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