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5,7-Dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-ylamine is a chemical compound with the molecular formula C6H7N5. It belongs to the class of triazolopyrimidines, which are heterocyclic compounds with a triazole ring fused to a pyrimidine ring. This specific compound features two methyl groups at the 5 and 7 positions of the triazolopyrimidine core, and an amine functional group at the 2 position. It is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various biologically active molecules. The compound's structure and properties make it a valuable intermediate in the development of new drugs and pharmaceuticals, as it can be further modified to create a range of compounds with different therapeutic effects.

7135-02-6

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7135-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7135-02-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,3 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7135-02:
(6*7)+(5*1)+(4*3)+(3*5)+(2*0)+(1*2)=76
76 % 10 = 6
So 7135-02-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H9N5/c1-4-3-5(2)12-7(9-4)10-6(8)11-12/h3H,1-2H3,(H2,8,11)

7135-02-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-amine

1.2 Other means of identification

Product number -
Other names 5,7-Dimethyl<1,2,4>triazolo<1,5-a>pyrimidin-2-amine

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:7135-02-6 SDS

7135-02-6Relevant academic research and scientific papers

Synthesis, crystal structure and herbicidal activity of a series of [1,2,4]triazolo[1,5-a]pyrimidine-2-sulfonamide compounds

Ma, Yi-Chao,Yu, Ying-Hui,Hou, Guang-Feng,Huang, Ji-Han,Gao, Jin-Sheng

, p. 829 - 843 (2016/07/06)

With the aim of obtaining efficient, safe and environmentally friendly green herbicide, a series of [1,2,4]triazolo[1,5-a]pyrimidine-2-sulfonamide compounds (8a-8f) were synthesized by reacting 2-amino-5,7-(bis-substituted)- 1,2,4-triazolo[1,5-a]pyrimidine (4a and 4b) with 2-substituted-6-trifluoromethyl-benzenesulfonyl chloride (7a-7c). And their structures were characterized by H-NMR, C-NMR, HRMS, FTIR, single-crystal X-ray diffraction, elemental analysis. Moreover, their herbicidal activities against six species of weeds were evaluated. Three target compounds such as 8a, 8c and 8e, exhibited significant postemergence herbicidal activity against some common dicotyledons and monocotyledons under different concentrations. The structure and activity relationship is discussed based on the herbicidal performances of the compounds with different substituents. The investigation results indicated that the above structures could serve as lead compounds for the development of new herbicides.

Synthesis and reactions of [1,2,4]triazolo[1,5-a]pyrimidinium-2-aminides

Bishop, Brian C.,Marley, Hugh,Preston, Peter N.,Wright, Stanley H. B.

, p. 1527 - 1532 (2007/10/03)

[1,2,4]Triazolo[1,5-a]pyrimidinium-2-amides were synthesised by treating an appropriate triazolo[1,5-a]pyrimidinium salt with sodium hydroxide or from the reaction of 4-alkyl-3,5-diamino-1,2,4-triazoles with pentane-2,4-dione or 1,1,3,3-tetramethoxypropan

A unique fourfold intramolecular hydrogen bonding stabilises the structure of trans-bis(2-amino-5,7-dimethyl[1,2,4]triazolo[1,5-a]pyrimidine- N3)aquatrichlororuthenium(III) monohydrate

Velders, Aldrik H.,Ugozzoli, Franco,Biagini-Cingi, Marina,Manotti-Lanfredi, Anna M.,Haasnoot, Jaap G.,Reedijk, Jan

, p. 213 - 215 (2007/10/03)

The X-ray structure of the potential antitumour complex trans- [RuCl3(H2O)(admtp)2] · H2O (admtp = 2-amino-5,7- dimethyl[1,2,4]triazolo[1,5-a]pyrimidine) shows unique and very interesting intramolecular hydrogen-bonding properties with the non-bridgehead pyrimidinic nitrogen atom of admtp acting as hydrogen acceptor and the amino group acting as hydrogen donor.

Sulfonamides derived from substituted 2-amino-1,2,4-triazolo (1,5-a) pyrimidines and compositions and methods of controlling undesired vegetation

-

, (2008/06/13)

Novel compounds, e.g., N-(5,7-dimethyl-1,2,4-triazolo [1,5-a]pyrimidin-2-yl)-2-thiophene sulfonamide and their compositions and use in the control of weeds.

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