1029720-98-6

Basic information

• Product Name: Ethyl 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-2-carboxylate
• Synonyms: Ethyl 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-2-carboxylate;Pyrazolo[1,5-a]pyrazine-2-carboxylic acid, 4,5,6,7-tetrahydro-, ethyl ester
• CAS NO: 1029720-98-6
• Molecular Formula: C₉H₁₃N₃O₂
• Molecular Weight: 195.21842
• Mol File: 1029720-98-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 365.0±42.0 °C(Predicted)
• Appearance: /
• Density: 1.35±0.1 g/cm3(Predicted)
• PKA: 8.38±0.20(Predicted)
• CAS DataBase Reference: Ethyl 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-2-carboxylate(1029720-98-6)
• EPA Substance Registry System: Ethyl 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-2-carboxylate(1029720-98-6)

Safety Data

• Hazardous Substances Data: 1029720-98-6(Hazardous Substances Data)

Usage

General Description

Ethyl 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-2-carboxylate is a chemical compound with the molecular formula C10H15N3O2. It is a heterocyclic compound that contains a pyrazine ring and an ethyl ester group. Ethyl 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-2-carboxylate may have potential applications in the pharmaceutical industry, as it exhibits interesting biological activities. However, further research is necessary to fully understand its properties and potential uses. As with any chemical compound, it is important to handle and use ethyl 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-2-carboxylate with care and in accordance with proper safety protocols.

Upstream product

• 934630-06-5 4-(benzyloxy-carbonyl)-2-piperazinecarboxylic acid 
• 1065066-04-7 5-benzyl-2-ethyl 6,7-dihydro-4H-pyrazolo[1,5-a]pyrazine-2,5-dicarboxylate 
• 1338563-24-8 ethyl 5-(2-nitrophenylsulfonyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-2-carboxylate 
• 1338563-23-7 N-(2-chloroethyl)-2-nitro-N-(prop-2-ynyl)benzenesulfonamide 

Downstream Products

• 1338563-35-1 ethyl 5-(4-methoxybenzoyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-2-carboxylate 
• 1338563-37-3 5-(4-methoxybenzoyl)-N-(tetrahydro-2H-pyran-2-yloxy)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-2-carboxamide 
• 1338562-86-9 N-hydroxy-5-(4-methoxybenzoyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-2-carboxamide 
• 1338563-36-2 5-(4-methoxybenzoyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-2-carboxylic acid 

Relevant articles and documents

Histone deacetylase inhibitors derived from 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine and related heterocycles selective for the HDAC6 isoform

Acyl derivatives of 4-(aminomethyl)-N-hydroxybenzamide are potent sub-type selective HDAC6 inhibitors. Constrained heterocyclic analogs based on 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine show further enhanced HDAC6 selectivity and inhibitory activity in ce

SUBSTITUTED PYRROLIDINE AMIDES, THE PRODUCTION THEREOF, AND THE USE THEREOF AS MEDICATIONS

The object of the present invention is novel substituted pyrrolidine amides of the general formula (I) in which D, L. E, G, J, M, L1, L2, R4, and R5 are defined as in the specification, the tautomers, enantiomers, diastereomers, mixtures, and salts thereof, particularly physiologically tolerated salts with inorganic or organic acids or bases having valuable properties.