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1,2,4-Triazolo[4,3-a]pyridine, 5,6,7,8-tetrahydro-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89569-61-9

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89569-61-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89569-61-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,6 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89569-61:
(7*8)+(6*9)+(5*5)+(4*6)+(3*9)+(2*6)+(1*1)=199
199 % 10 = 9
So 89569-61-9 is a valid CAS Registry Number.

89569-61-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyridine

1.2 Other means of identification

Product number -
Other names HMS2396H17

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:89569-61-9 SDS

89569-61-9Downstream Products

89569-61-9Relevant academic research and scientific papers

Organometallic Complex, Light-Emitting Element, Light-Emitting Device, Electronic Device, and Lighting Device

-

, (2013/02/28)

An organometallic complex emitting blue phosphorescence which can be manufactured inexpensively is provided. An organometallic complex in which nitrogen at the 1-position of a 5-aryl-4H-1,2,4-triazole derivative is coordinated to a Group 9 metal or a Group 10 metal, the aryl group is bonded to the Group 9 metal or the Group 10 metal, and the 5-aryl-4H-1,2,4-triazole derivative is a 3-aryl-5,6,7,8-tetrahydro-4H-[1,2,4]triazolo[4,3-a]pyridine derivative is provided. The organometallic complex emits green to blue phosphorescence and has a cost advantage.

Reaction Between Ethyl ω-Chloroalkylimidates and Hydrazides

Bonanomi, Michele,Baiocchi, Leandro

, p. 1657 - 1660 (2007/10/02)

It is already known that ethyl ω-chloroalkylimidate hydrochlorides and aroyl hydrazides gave, when reacted together in boiling ethanol, 2-aryl-5-ω-haloalkyl-1,3,4-oxadiazoles.It has now been found that the reaction follows a different course in the presence of triethylamine.In particular, 2-aryl-5,6,7,8-tetrahydro-1,2,4-triazolopyridines were obtained from ethyl δ-chlorovalerimidate, whereas N-aroylaminoiminopyrrolidines are the products obtained from ethyl γ-chlorobutyrimidate.A similar case, in which the closure of the triazole ring to obtain a dihydropyrrolotriazole was found to be more difficult than the corresponding closure to a tetrahydrotriazolopyridine, is described.Also the reaction between the imidates and carbethoxyhydrazine, which gives piperidine and pyrrolidine derivatives, is reported.

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