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1-(1,2-dimethyl-1H-pyrrolo[3,2-c]cinnolin-3-yl)ethanone is a complex chemical compound that features a unique molecular structure. It is a derivative of ketone with a pyrrolo[3,2-c]cinnoline skeleton and a 1-(1,2-dimethyl) substitution at the 1-position. 1-(1,2-dimethyl-1H-pyrrolo[3,2-c]cinnolin-3-yl)ethanone holds potential for various applications in fields such as organic synthesis and medicinal chemistry, with its specific uses and properties dependent on the context. 1-(1,2-dimethyl-1H-pyrrolo[3,2-c]cinnolin-3-yl)ethanone's distinctive structure and functional groups make it a promising candidate for further research and exploration within the chemical sciences.

82157-88-8

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82157-88-8 Usage

Uses

Used in Organic Synthesis:
1-(1,2-dimethyl-1H-pyrrolo[3,2-c]cinnolin-3-yl)ethanone is used as an intermediate in the synthesis of various organic compounds. Its unique structure and functional groups allow for a range of chemical reactions, making it a valuable component in the creation of new molecules with potential applications in various industries.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(1,2-dimethyl-1H-pyrrolo[3,2-c]cinnolin-3-yl)ethanone is used as a building block for the development of novel pharmaceuticals. Its structural diversity and potential for modification make it an attractive candidate for the design of new drugs targeting specific biological pathways or receptors.
Used in Chemical Research:
1-(1,2-dimethyl-1H-pyrrolo[3,2-c]cinnolin-3-yl)ethanone is also utilized as a subject of study in chemical research. Its complex structure and functional groups provide opportunities for scientists to investigate new reaction mechanisms, explore its reactivity, and potentially discover new properties or applications for 1-(1,2-dimethyl-1H-pyrrolo[3,2-c]cinnolin-3-yl)ethanone.
Used in Pharmaceutical Industry:
Within the pharmaceutical industry, 1-(1,2-dimethyl-1H-pyrrolo[3,2-c]cinnolin-3-yl)ethanone is used as a key component in the development of new drugs. Its unique structure and potential for modification make it a valuable asset in the creation of innovative therapeutic agents that can address unmet medical needs.
Used in Material Science:
1-(1,2-dimethyl-1H-pyrrolo[3,2-c]cinnolin-3-yl)ethanone may also find applications in material science, where its unique properties could be harnessed to develop new materials with specific characteristics, such as improved stability, reactivity, or selectivity in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 82157-88-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,5 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82157-88:
(7*8)+(6*2)+(5*1)+(4*5)+(3*7)+(2*8)+(1*8)=138
138 % 10 = 8
So 82157-88-8 is a valid CAS Registry Number.

82157-88-8SDS

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 1-(1,2-dimethylpyrrolo[3,2-c]cinnolin-3-yl)ethanone

1.2 Other means of identification

Product number -
Other names -

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

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More Details:82157-88-8 SDS

82157-88-8Downstream Products

82157-88-8Relevant academic research and scientific papers

POLYCONDENSED NITROGEN HETEROCYCLES. PART XI. 1,3-DISUBSTITUTED 2-METHYLPYRROLOCINNOLINE AND 2-ACETYL-3-METHYLPYRROLOBENZOTRIAZINE

Dattolo, Gaetano,Cirrincione, Girolamo,Almerico, Anna Maria,D'Asdia, Isabella,Aiello, Enrico

, p. 681 - 686 (2007/10/02)

The diazotization of 1,3-disubstituted 2-methyl-5-(2-aminophenyl)pyrroles (2) and the intramolecular coupling reaction of the resulting diazonium salts lead to pyrrolobenzotriazine 4 when R = H.Compound 3d inhibited the germination of seeds

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