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2,3-Dihydro-2-methyl-3-methylenepyrazino[1,2-a]indole-1,4-dione, also known as 2-methyl-3-methylenepyrazinoindole-1,4-dione, is a heterocyclic chemical compound with the molecular formula C12H10N2O2. It belongs to the indole family and features a pyrazine ring. 2,3-Dihydro-2-methyl-3-methylenepyrazino[1,2-a]indole-1,4-dione has been the subject of research for its potential pharmacological properties, particularly its effects on the central nervous system. It is also considered in the field of medicinal chemistry for its possible role in the development of new drugs. The specific biological activities and potential applications of 2,3-Dihydro-2-methyl-3-methylenepyrazino[1,2-a]indole-1,4-dione are still under investigation.

19079-11-9

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19079-11-9 Usage

Uses

Used in Pharmaceutical Research:
2,3-Dihydro-2-methyl-3-methylenepyrazino[1,2-a]indole-1,4-dione is used as a compound of interest in pharmaceutical research for its potential pharmacological properties. It is being studied for its effects on the central nervous system, which could lead to the development of new drugs targeting neurological conditions.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,3-Dihydro-2-methyl-3-methylenepyrazino[1,2-a]indole-1,4-dione is used as a starting point for the synthesis of new drug candidates. Its unique structure and potential biological activities make it a valuable component in the search for novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 19079-11-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,7 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19079-11:
(7*1)+(6*9)+(5*0)+(4*7)+(3*9)+(2*1)+(1*1)=119
119 % 10 = 9
So 19079-11-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H10N2O2/c1-8-12(16)15-10-6-4-3-5-9(10)7-11(15)13(17)14(8)2/h3-7H,1H2,2H3

19079-11-9SDS

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 2-methyl-3-methylidenepyrazino[1,2-a]indole-1,4-dione

1.2 Other means of identification

Product number -
Other names 1-methyl-2-methylene-3,10-dioxopiperazino<1,2-a>indole

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:19079-11-9 SDS

19079-11-9Downstream Products

19079-11-9Relevant academic research and scientific papers

The Biosynthetic Incorporation of Phenylalanine into Gliotoxin

Johns, Nicholas,Kirby, Gordon W.

, p. 1487 - 1490 (2007/10/02)

When mixtures of DL--m-tyrosine and DL-phenylalanine were fed to cultures of Gliocladium deliquescens good incorporation (4.9 and 1.6percent in separate experiments) of (14)C and negligible incorporation (ca. 0.04percent) of (3)H into the derived gliotoxin (2) was observed.Incorporation of DL--, DL--, and L--phenylalanine into gliotoxin occured without loss of tritium.Degradation of the gliotoxin gave, in each case, bis(anhydro-dethio)gliotoxin (3) and dehydrogliotoxin (4) having a tritium content indicating that the incorporation of phenylalanine had occured without migration of tritium.These results, taken together, show that neither m-tyrosine (3'-hydroxyphenylalanine) nor any other hydroxybenzene derivative can be an obligatory intermediate on the biosynthetic pathway from phenylalanine to gliotoxin.The possible involvement of arene oxides in gliotoxin biosyhthesis is discussed.

Synthesis of dehydroamino acids and didehydrodioxopiperazines and their conversion into α-mercapto-α-amino acid derivatives

Herscheid, Jacobus D. M.,Scholten, Henk P. H.,Tijhuis, Marian W.,Ottenheim, Harry C. J.

, p. 73 - 78 (2007/10/02)

A synthesis of α,β-dehydroamino acid derivatives 12 is described, which is of possible general applicability and might be useful for the preparation of peptides which have such a moiety in their sequence.I addition, several didehydrodioxopiperazines (13-1

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