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5825-71-8

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5825-71-8 Usage

General Description

Dimethyl Pyrazolo[1,5-a]pyridine-2,3-dicarboxylate is an organic compound categorized under the chemical class of pyrazolopyridines. It is synthesized from a pyrazole derivative in presence of a suitable oxidant through a method known as oxidative cyclization. This chemical compound is typically used in the field of pharmaceuticals, where it may be utilized to create active pharmaceutical ingredients for medications. Its intricate organic structure plays a crucial role in its reactivity and usefulness in various reactions. The specifics of its safety, toxicity, and environmental impact, however, are not widely documented and may vary depending on its application and handling.

Check Digit Verification of cas no

The CAS Registry Mumber 5825-71-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,2 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5825-71:
(6*5)+(5*8)+(4*2)+(3*5)+(2*7)+(1*1)=108
108 % 10 = 8
So 5825-71-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N2O4/c1-16-10(14)8-7-5-3-4-6-13(7)12-9(8)11(15)17-2/h3-6H,1-2H3

5825-71-8SDS

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 Dimethyl Pyrazolo[1,5-a]pyridine-2,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names DIMETHYL PYRAZOLO[1,5-A]PYRIDINE-2,3-DICARBOXYLATE

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:5825-71-8 SDS

5825-71-8Relevant articles and documents

Study on selectivity in the reaction of 2-substituted pyridinium-N-imines with dimethyl acetylenedicarboxylate

Supranovich, Vyacheslav I.,Vorob'ev, Aleksey Yu.,Borodkin, Gennady I.,Gatilov, Yury V.,Shubin, Vyacheslav G.

supporting information, p. 1093 - 1096 (2016/03/09)

Reactions of 2-X-pyridinium-N-imines (X = F, Cl, Br, CN, OPh, NH2, N-morpholine) with dimethyl acetylenedicarboxylate (DMAD) have been studied. In the case of X = Cl, Br, CN, OPh both 7-substituted- and 7-H-pyrazolo[1,5-a]pyridines are formed. The 7-H/7-X ratio usually increases with the growing solvent polarity. The reaction of N-amino-2-iminopyridine with DMAD gives substituted pyrido[1,2-b][1,2,4]triazine.

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