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Pyrrolo[1,2-a]pyrazine, 3,4-dihydro(9CI) is a bicyclic heteroaromatic chemical compound with the molecular formula C7H6N2. It features both a pyrrole and a pyrazine ring, and the 3,4-dihydroprefix signifies that the double bonds in the pyrrole ring are reduced to single bonds. This unique structure endows it with potential biological activity and makes it a promising candidate for various applications in the pharmaceutical and chemical industries.

71257-37-9

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71257-37-9 Usage

Uses

Used in Pharmaceutical Industry:
Pyrrolo[1,2-a]pyrazine, 3,4-dihydro(9CI) is used as a building block for the synthesis of various heterocyclic compounds. Its unique structure and potential biological activity make it a valuable component in the development of new drugs, potentially contributing to the creation of innovative therapeutic agents.
Used in Chemical Industry:
In the chemical industry, Pyrrolo[1,2-a]pyrazine, 3,4-dihydro(9CI) may have potential use in the development of new agrochemicals. Its complex structure and properties could be harnessed to create novel compounds with applications in agriculture, such as pesticides or herbicides.
Further Research:
Due to its complex structure and potential biological activity, Pyrrolo[1,2-a]pyrazine, 3,4-dihydro(9CI) requires additional research and studies to fully understand its properties and potential applications. This will enable the development of more targeted and effective uses in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 71257-37-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,2,5 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 71257-37:
(7*7)+(6*1)+(5*2)+(4*5)+(3*7)+(2*3)+(1*7)=119
119 % 10 = 9
So 71257-37-9 is a valid CAS Registry Number.

71257-37-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dihydropyrrolo[1,2-a]pyrazine

1.2 Other means of identification

Product number -
Other names MGVILGGQOXEHIW-UHFFFAOYSA

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:71257-37-9 SDS

71257-37-9Relevant academic research and scientific papers

1,2,3,4-tetrahydropyrrolo-[1,2-a]-pyrazine derivatives

-

, (2008/06/13)

1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine derivatives having the formula (Formula I) STR1 and therapeutically acceptable acid addition salts thereof (Formula I.HX), wherein: R1 =hydrogen or acyl groups; and R2 =hydrogen or substituted

Bridged 2,2'-biazole derivatives by 1,3-dipolar cycloaddition

De Pablo,Gandasegui,Vaquero,Garcia Navio,Alvarez-Builla

, p. 8793 - 8800 (2007/10/02)

Azomethine ylides derived from 3,4-dihydropyrrolo[1,2-a]pyrazinium salts undergo 1,3-dipolar cycloaddition reactions to yield 5,6-dihydrodipyrrolo[1,2-a:2',1'-c]-pyrazine and 5,6-dihydroimidazo[1,2-a]pyrrolo[2,1-c]pyrazin-4-inium-2-olate and 2-thiolate de

AZACYCLOALKANES. XXVI. NEW METHOD FOR THE SYNTHESIS OF 3,4-DIHYDROPYRROLOPYRAZINES

Likhosherstov, A. M.,Peresada, V. P.,Skoldinov, A. P.

, p. 393 - 397 (2007/10/02)

A new general method was developed for the synthesis of 3,4-dihydropyrrolopyrazines by condensation of 2,5-dialkoxy-2-dialkoxymethyltetrahydrofurans with aliphatic 1,2-diamines in acetic acid.In the reaction with unsymmetrical diamines the isomers with the substituents more distant from the pyrrole ring are formed preferentially.

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