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ETHYL 7-(PYRIDIN-3-YL)PYRAZOLO[1,5-A]PYRIMIDINE-3-CARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78562-03-5

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78562-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78562-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,6 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78562-03:
(7*7)+(6*8)+(5*5)+(4*6)+(3*2)+(2*0)+(1*3)=155
155 % 10 = 5
So 78562-03-5 is a valid CAS Registry Number.

78562-03-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 7-pyridin-3-ylpyrazolo[1,5-a]pyrimidine-3-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:78562-03-5 SDS

78562-03-5Downstream Products

78562-03-5Relevant academic research and scientific papers

Vinylation of α-Aminoazoles with Triethylamine: A General Strategy to Construct Azolo[1,5-a]pyrimidines with a Nonsubstituted Ethylidene Fragment

Gao, Qinghe,Sun, Zhenhua,Xia, Qinfei,Li, Ruonan,Wang, Wenlong,Ma, Siwei,Chai, Yixin,Wu, Manman,Hu, Wei,ábrányi-Balogh, Péter,Keserü, Gy?rgy M.,Han, Xinya

supporting information, p. 2664 - 2669 (2021/04/12)

A new general synthesis of pharmaceutically important azolo[1,5-a]pyrimidines starting from widely available 3(5)-aminoazoles, aldehydes, and triethylamine is developed. The key is to enable the vinylation reaction that allows the in situ generation of elusive acyclic enamines and the subsequent annulation reaction to occur. This direct and practical strategy is capable of constructing a range of 5,6-unsubstituted pyrazolo[1,5-a]pyrimidines and [1,2,4]triazolo[1,5-a]pyrimidines. More importantly, this protocol provides a concise synthetic route to prepare the clinically used zaleplon.

Synthetic method of pyrazolopyrimidine compound

-

Paragraph 0010; 0077-0079, (2021/06/12)

The invention discloses a synthesis method of a pyrazolopyrimidine compound, and belongs to the technical field of organic synthesis. According to the technical scheme, the method is characterized by comprising the following steps: dissolving an aldehyde

Synthesis of a new series of pyrazolo[1,5-a]pyrimidines structurally related to zaleplon

Baraldi, Pier Giovanni,Fruttarolo, Francesca,Tabrizi, Mojgan Aghazadeh,Romagnoli, Romeo,Preti, Delia,Ongini, Ennio,El-Kashef, Hussein,Carrion, Maria Dora,Borea, Pier Andrea

, p. 355 - 361 (2008/04/12)

(Chemical Equation Presented) The reaction between 3-(dimethylamino)/3,3- bis(methylthio)-1-(substituted)prop-2-en-1-ones and 4-substituted-5-amino-1H- pyrazoles afforded new pyrazole[1,5-a]pyrimidines structurally related to Zaleplon. The chemical modifications introduced at the 3-, 5-, and 7-positions of the bicyclic structure revealed new promising candidates for the treatment of sleep disorders.

Substituted pyrazolo (1,5-a)pyrimidines and their use as anxiolytic agents

-

, (2008/06/13)

This disclosure describes substituted pyrazolo[1,5-a]pyrimidines which possess anxiolytic activity.

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