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6-Methyl-1-aza-9H-carbazole is a chemical compound with the molecular formula C13H11N, belonging to the carbazole family of tricyclic aromatic hydrocarbons. It features a methyl group on the 6th carbon atom and is known for its unique structural properties. 6-Methyl-1-aza-9H-carbazole has garnered interest in the fields of organic chemistry and materials science for its potential applications, including the development of organic semiconductors and as a building block for synthesizing complex organic molecules. Its distinctive structure and properties also suggest possible pharmaceutical applications, although further research is required to explore these possibilities fully.

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  • 108349-67-3 Structure
  • Basic information

    1. Product Name: 6-Methyl-1-aza-9H-carbazole
    2. Synonyms: 6-Methyl-1-aza-9H-carbazole
    3. CAS NO:108349-67-3
    4. Molecular Formula: C12H10N2
    5. Molecular Weight: 182.2212
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 108349-67-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-Methyl-1-aza-9H-carbazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-Methyl-1-aza-9H-carbazole(108349-67-3)
    11. EPA Substance Registry System: 6-Methyl-1-aza-9H-carbazole(108349-67-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 108349-67-3(Hazardous Substances Data)

108349-67-3 Usage

Uses

Used in Organic Chemistry:
6-Methyl-1-aza-9H-carbazole is used as a building block for the synthesis of complex organic molecules due to its unique structure and properties, contributing to the advancement of organic chemistry.
Used in Materials Science:
In the field of materials science, 6-Methyl-1-aza-9H-carbazole is utilized for the development of organic semiconductors, leveraging its structural properties to enhance the performance of these materials.
Used in Pharmaceutical Applications:
6-Methyl-1-aza-9H-carbazole holds potential for pharmaceutical applications due to its unique structure and properties, although further research is necessary to fully understand and realize its potential in this industry.

Check Digit Verification of cas no

The CAS Registry Mumber 108349-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,3,4 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 108349-67:
(8*1)+(7*0)+(6*8)+(5*3)+(4*4)+(3*9)+(2*6)+(1*7)=133
133 % 10 = 3
So 108349-67-3 is a valid CAS Registry Number.

108349-67-3Downstream Products

108349-67-3Relevant articles and documents

Ir-Catalyzed Intramolecular Transannulation/C(sp2)-H Amination of 1,2,3,4-Tetrazoles by Electrocyclization

Das, Sandip Kumar,Roy, Satyajit,Khatua, Hillol,Chattopadhyay, Buddhadeb

supporting information, p. 8429 - 8433 (2018/07/09)

An efficient strategy for the intramolecular denitrogenative transannulation/C(sp2)-H amination of 1,2,3,4-tetrazoles bearing C8-substituted arenes, heteroarenes, and alkenes is described. The process involves the generation of the metal-nitrene intermediate from tetrazole by the combination of [CpIrCl2]2 and AgSbF6. It has been shown that the reaction proceeds via an unprecedented electrocyclization process. The method has been successfully applied for the synthesis of a diverse array of α-carbolines and 7-azaindoles.

CaMKII INHIBITORS AND USES THEREOF

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Paragraph 00358-00362; 00368-00369, (2016/05/02)

The present invention provides compounds useful as inhibitors of Ca2+/calmodulin-dependent protein kinase (CaMKII), compositions thereof, and methods of using the same.

CaMKII INHIBITORS AND USES THEREOF

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Paragraph 00247-00248; 00258-00259, (2014/09/29)

The present invention provides compounds useful as inhibitors of Ca2+/calmodulindependent protein kinase (CaMKII), compositions thereof, and methods of using the same. Cardiovascular disease remains the number one cause of death in developed countries. Furthermore, incidence of cardiovascular disease has increased dramatically in developing countries. Although cardiovascular disease usually affects older adults, the antecedents of cardiovascular disease, notably atherosclerosis, begin in early life, making primary prevention efforts necessary from childhood.

A short entry into the pyrido[2,3-b] indole ring system. Synthesis of the tetracyclic segment of the marine antitumor agents: Grossularines-1 and -2

Achab, Said,Guyot, Michele,Potier, Pierre

, p. 2127 - 2130 (2007/10/02)

A new method for the synthesis of substituted pyrido[2,3-b] indoles (α-carbolines) (14, 27-31), featuring Pd-catalyzed cross coupling between pyridine and aniline derivatives and subsequent intramolecular cylization, has been developed. This method provid

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