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9-Bromo-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one is an organic compound characterized by a complex multi-cyclic structure, featuring a bromo substituent and two nitrogenous heterocyclic rings, namely quinazolinone and triazolo. With the chemical formula C8H5BrN4O, 9-Bromo-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one is known for its functional groups that make it a versatile entity in chemical reactions and binding, primarily utilized in the fields of organic synthesis and pharmaceuticals.

882517-92-2

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882517-92-2 Usage

Uses

Used in Organic Synthesis:
9-Bromo-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one is used as a synthetic intermediate for the creation of various organic compounds. Its unique structure and functional groups facilitate multiple chemical reactions, making it a valuable component in the synthesis of new molecules with potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 9-Bromo-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one is used as a key building block in the development of novel drugs. Its heterocyclic rings and functional groups can be modified to create new pharmaceutical agents with specific therapeutic properties, targeting a range of diseases and medical conditions.
The properties, safety data, and potential toxicological characteristics of 9-Bromo-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one are typically industry-specific, and its assessment often requires advanced chemical analysis to ensure safe and effective use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 882517-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,5,1 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 882517-92:
(8*8)+(7*8)+(6*2)+(5*5)+(4*1)+(3*7)+(2*9)+(1*2)=202
202 % 10 = 2
So 882517-92-2 is a valid CAS Registry Number.

882517-92-2SDS

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 9-Bromo-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one

1.2 Other means of identification

Product number -
Other names 9-bromo-3H-[1,2,4]triazolo[1,5-c]quinazolin-5-one

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:882517-92-2 SDS

882517-92-2Relevant academic research and scientific papers

The discovery and unique pharmacological profile of RO4938581 and RO4882224 as potent and selective GABAA α5 inverse agonists for the treatment of cognitive dysfunction

Knust, Henner,Achermann, Guido,Ballard, Theresa,Buettelmann, Bernd,Gasser, Rodolfo,Fischer, Holger,Hernandez, Maria-Clemencia,Knoflach, Frederic,Koblet, Andreas,Stadler, Heinz,Thomas, Andrew W.,Trube, Gerhard,Waldmeier, Pius

scheme or table, p. 5940 - 5944 (2010/05/18)

Lead optimisation of the imidazo[1,5-a][1,2,4]-triazolo[1,5-d][1,4]benzodiazepine class led to the identification of two clinical leads [RO4882224 (11) and RO4938581 (44)] functioning as novel potent and selective GABAA α5 inverse agonists. The unique pharmacological profiles and optimal pharmacokinetic profiles resulted in in vivo activity in selected cognition models.

Substituted imidazol[1,5-A][1,2,4]triazolo[1,5-D][1,4]benzodiazepine derivatives

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Page/Page column 9, (2008/06/13)

The present invention is concerned with substituted imidazo[1,5-a][1,2,4]triazolo[1,5-d][1,4]benzodiazepine derivatives of formula I wherein R1 is hydrogen, halogen, lower alkyl, lower alkynyl, cycloalkyl, heterocycloalkyl, benzyl, cyano, lower

Halogen substituted imidazol[1,5-A][1,2,4]triazolo[1,5-D][1,4]benzodiazepine derivatives

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Page/Page column 12, (2008/06/13)

The invention relates to halogen substituted imidazo[1,5-a][1,2,4]triazolo[1,5-d][1,4]benzodiazepine derivatives of formula I wherein R1, R2, R3, R4 and n are as defined in the specification and to pharmaceutica

Substituted imidazo[1,5-a][1,2,4]triazolo[1,5-d][1,4]benzodiazepine derivatives

-

Page/Page column 18, (2010/10/20)

The present invention is concerned with a method of treating a disease selected from the group consisting of cognitive disorders, anxiety, Alzheimer's disease, and schizophrenia comprising administering a therapeutically effective amount of a substituted

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