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4,5,6-trimethyl-1,2,3-triazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33209-85-7

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33209-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33209-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,2,0 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33209-85:
(7*3)+(6*3)+(5*2)+(4*0)+(3*9)+(2*8)+(1*5)=97
97 % 10 = 7
So 33209-85-7 is a valid CAS Registry Number.

33209-85-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5,6-trimethyltriazine

1.2 Other means of identification

Product number -
Other names 4,5,6-Trimethyl-1,2,3-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:33209-85-7 SDS

33209-85-7Downstream Products

33209-85-7Relevant academic research and scientific papers

Reactions of N-Aminopyrazoles with Halogenating Reagents and Synthesis of 1,2,3-Triazines

Ohsawa, Akio,Kaihoh, Terumitsu,Itoh, Takashi,Okada, Mamiko,Kawabata, Chikako,et al.

, p. 3838 - 3848 (2007/10/02)

Reactions of N-aminopyrazoles with halogenating reagents (Cl2, Br2, I2, BrCl, ICl, IBr, N-chlorosuccinimide, and N-bromosuccinimide) were examined.Some of these reagents preferentially lead to oxidation of the amino group to give the corresponding 1,2,3-triazines as major products, while others mainly gave either or both of 1-amino-4-halopyrazoles and 5-halo-1,2,3-triazines as the result of halogenation of the 4-position of the pyrazole ring prior to the oxidation of the amino group.In some cases, the oxidation of the amino group and the halogenation of the pyrazole ring proceeded concurrently to form not only the unhalogenated triazines but also the 1-amino-4-halopyrazoles and the 5-halotriazines.Various reagents and reaction conditions were explored to utilize the reaction for the synthesis of halogenated and unhalogenated 1,2,3-triazines.Keywords - 1,2,3-triazine; halo-1,2,3-triazine; pyrazole; 1-aminopyrazole; 1-aminohalopyrazole; synthesis; oxidation; halogenation; ring expansion

Oxidation of 1-Aminopyrazoles and Synthesis of 1,2,3-Triazines

Ohsawa, Akio,Arai, Heihachiro,Ohnishi, Hidefumi,Itoh, Takashi,Kaihoh, Terumitsu,et al.

, p. 5520 - 5523 (2007/10/02)

Unsubstituted and various substituted monocyclic 1,2,3-triazines were synthesized from 1-aminopyrazoles by oxidation with lead tetraacetate, lead dioxide-CF3CO2H, and/or nickel peroxide-AcOH.

1,2,3-Triazines,III. - Synthesis of N-Aminopyrazoles and their Oxidation to 1,2,3-Triazines. Molecular Structure of 1,2,3-Triazine

Neunhoeffer, Hans,Clausen, Monika,Voetter, Hans-Dieter,Ohl, Harald,Krueger, Carl,Angermund, K.

, p. 1732 - 1751 (2007/10/02)

Oxidation of the N-aminopyrazoles 4a-i affords the 1,2,3-triazines 5a-i.Spectra and reactions - such as oxidation, reduction, and cycloaddition reactions - of some 1,2,3-triazines 5 are described.The X-ray analysis of 5a is presented.

Synthesis, Oxidation, and Reduction of Monocyclic 1,2,3-Triazines

Ohsawa, Akio,Arai, Heihachiro,Ohnishi, Hidefumi,Igeta, Hiroshi

, p. 1182 - 1183 (2007/10/02)

Alkyl substituted monocyclic 1,2,3-triazines and their 1- and 2-oxides have been synthesized; catalytic reduction (on Pd-C) of the triazines afforded their 2,5-dihydro compounds.

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