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400079-96-1

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400079-96-1 Usage

Description

4H,9H-DIPYRAZOLO[1,5-A:1,5-D]PYRAZINE-4,9-DIOL is a heterocyclic chemical compound characterized by a pyrazine ring system and two hydroxyl groups. With the molecular formula C8H6N6O2, this compound serves as a versatile building block in organic synthesis and pharmaceutical research, leveraging its unique structural and chemical properties for the development of new drugs and molecules.

Uses

Used in Organic Synthesis:
4H,9H-DIPYRAZOLO[1,5-A:1,5-D]PYRAZINE-4,9-DIOL is used as a key intermediate in organic synthesis for the creation of complex organic molecules. Its pyrazine ring system and hydroxyl groups facilitate various chemical reactions, enabling the formation of a wide range of compounds with diverse applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4H,9H-DIPYRAZOLO[1,5-A:1,5-D]PYRAZINE-4,9-DIOL is utilized as a building block for the synthesis of bioactive molecules with potential therapeutic applications. Its unique structure and chemical properties make it a valuable component in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Drug Discovery and Development:
4H,9H-DIPYRAZOLO[1,5-A:1,5-D]PYRAZINE-4,9-DIOL holds promise in drug discovery and development due to its potential biological activity. Researchers can explore its interactions with biological targets, such as enzymes, receptors, or other proteins, to identify its potential therapeutic effects and develop new drugs based on its structure.
Used as a Reagent in Chemical Reactions:
4H,9H-DIPYRAZOLO[1,5-A:1,5-D]PYRAZINE-4,9-DIOL can also be employed as a reagent in chemical reactions for the formation of new compounds. Its pyrazine ring and hydroxyl groups can participate in various reaction mechanisms, such as condensation, substitution, or oxidation, to produce novel molecules with potential applications in different fields.

Check Digit Verification of cas no

The CAS Registry Mumber 400079-96-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,0,7 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 400079-96:
(8*4)+(7*0)+(6*0)+(5*0)+(4*7)+(3*9)+(2*9)+(1*6)=111
111 % 10 = 1
So 400079-96-1 is a valid CAS Registry Number.

400079-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,9-dihydrodipyrazolo[1,3-b:1',3'-e]pyrazine-4,9-diol

1.2 Other means of identification

Product number -
Other names 3B-048

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:400079-96-1 SDS

400079-96-1Upstream product

400079-96-1Downstream Products

400079-96-1Relevant articles and documents

Synthesis of Pyrroloimidazol-5-one, Pyrroloimidazol-5-one and Pyrrolopyrazol-6-one (Three Isomeric Azapyrrolizinones), by Pyrolysis of Meldrum's Acid Derivatives

McNab, Hamish

, p. 653 - 656 (2007/10/02)

Reaction of Meldrum's acid with the imidazole- and pyrazole-carbaldehydes (9)-(11) gave the condensation products (6), (7a), and (8) which were pyrolysed in the gas phase to give the title azaanalogues (2)-(4) of pyrrolizin-3-one (1), as air-sensitive yellow solids.

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