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3,6-di(pyridin-2-yl)-1,4-dihydro-1,2,4,5-tetrazine is a complex organic compound with the molecular formula C12H10N6. It is characterized by a central tetrazine ring, which is a six-membered ring containing four nitrogen atoms. The compound features two pyridin-2-yl groups attached to the 3rd and 6th positions of the tetrazine ring, with each pyridin-2-yl group being a pyridine ring with a nitrogen atom at the 2nd position. This molecule is of interest in chemical research due to its unique structure and potential applications in various fields, such as pharmaceuticals and materials science. Its synthesis and properties are subjects of ongoing study to explore its potential uses and interactions with other molecules.

1671-86-9

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1671-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1671-86-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,7 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1671-86:
(6*1)+(5*6)+(4*7)+(3*1)+(2*8)+(1*6)=89
89 % 10 = 9
So 1671-86-9 is a valid CAS Registry Number.

1671-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-dipyridin-2-yl-1,4-dihydro-1,2,4,5-tetrazine

1.2 Other means of identification

Product number -
Other names dihydrotetrazine

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:1671-86-9 SDS

1671-86-9Relevant academic research and scientific papers

Synthesis of Pyridazine and Pyrrole Analogues of 2-Aminotetralin as Potential Dopaminergics

Kocak, Ramazan,Dastan, Arif,Saracoglu, Nurullah

, p. 1489 - 1493 (2018)

Syntheses of pyridazine and pyrrole analogues of 2-aminotetralin starting from 3-cyclohexene-1-carboxylic acid are reported. All syntheses involve the following key steps: Curtius rearrangement for amine functionality, inverse electron demand Diels–Alder

Thermal generation of pentacenes from soluble 6,13-dihydro-6,13- ethenopentacene precursors by a Diels-Alder-retro-Diels-Alder sequence with 3,6-disubstituted tetrazines

Bula, Rafael P.,Oppel, Iris M.,Bettinger, Holger F.

experimental part, p. 3538 - 3542 (2012/06/15)

3,6-Substituted tetrazines 2 (a: R2 = 2-pyridyl or b: CO 2Me) react with 2,3,9,10-(R1)4-dihydro-6,13- ethenopentacene 3 in solution at elevated temperature to the corresponding pentacene 1 (a: R1 = H, b: OBn, c: F).

Synthesis and biological action of 3,4-disubstituted 5- arylsulphonylamine-1,2,4-triazoles

Modzelewska-Banachiewicz,Matosiuk

, p. 588 - 589 (2007/10/03)

The synthesis of 3,4-disubstituted 5-arylsulphonylamine-1,2,4-triazoles is described. The antimicrobial activities of the compounds were investigated as well as their acute toxicity.

BADANIA W DZIEDZINIE TIOAMIDOW I ICH POCHODNYCH IX. SYNTEZA POCHODNYCH 1,2,4,5-TETRAZYNY

Santus, Maria

, p. 183 - 188 (2007/10/02)

In reactions of N,N-disubstituted thioamides, derivatives of 4-thiobenzoylmorpholine, 1-thiobenzoylpiperidine and N1,N2-di(α-morpholinobenzylidene)azine, N1,N2-di(α-piperidinobenzylidene)azine also 4-(R-α-phenylaminobenzylidene)morpholinium and 1-(R-α-phenylaminobenzylidene)piperidinium iodides with hydrazine there was obtained a series compounds, derivatives of 1,2,4,5-tetrazine.Structures of obtained compounds have been determined by elemental analysis and on the ground of their UV and IR spectra.

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