What is the 3,6-diMethoxy-9H-carbazole?

3,6-diMethoxy-9H-carbazole is , while it's Molecular Formula is C14H13NO2. Used in Pharmaceutical Industry: 3,6-Dimethoxy-9H-carbazole is used as a potential active pharmaceutical ingredient for its possible antimicrobial, antiviral, and anticancer properties, which are common among carbazole compounds. Used in Chemical Research: 3,6-Dimethoxy-9H-carbazole is used as a research compound for studying the properties and potential applications of carbazole derivatives in various chemical and biological fields. Used in Material Science: 3,6-Dimethoxy-9H-carbazole is used as a component in the development of new materials, potentially benefiting from the unique structural and functional characteristics of carbazole compounds.

What is the CAS number for 3,6-diMethoxy-9H-carbazole?

The CAS number of 3,6-diMethoxy-9H-carbazole is 57103-01-2.

What is 3,6-diMethoxy-9H-carbazole (57103-01-2) used for?

3,6-Dimethoxy-9H-carbazole is a chemical compound that belongs to the carbazole family, which are heterocyclic organic compounds. It is composed of carbon, hydrogen, and oxygen atoms, and features functional groups such as methoxy groups and aromatic rings. Although its specific applications and properties are not extensively studied, carbazole compounds are known for their biological activities, including antimicrobial, antiviral, and anticancer properties, suggesting that 3,6-Dimethoxy-9H-carbazole could be utilized in similar medicinal or chemical applications.

What is the 3,6-diMethoxy-9H-carbazole?

3,6-diMethoxy-9H-carbazole is , while it's Molecular Formula is C14H13NO2. Used in Pharmaceutical Industry: 3,6-Dimethoxy-9H-carbazole is used as a potential active pharmaceutical ingredient for its possible antimicrobial, antiviral, and anticancer properties, which are common among carbazole compounds. Used in Chemical Research: 3,6-Dimethoxy-9H-carbazole is used as a research compound for studying the properties and potential applications of carbazole derivatives in various chemical and biological fields. Used in Material Science: 3,6-Dimethoxy-9H-carbazole is used as a component in the development of new materials, potentially benefiting from the unique structural and functional characteristics of carbazole compounds.

What is the CAS number for 3,6-diMethoxy-9H-carbazole?

The CAS number of 3,6-diMethoxy-9H-carbazole is 57103-01-2.

What is 3,6-diMethoxy-9H-carbazole (57103-01-2) used for?

3,6-Dimethoxy-9H-carbazole is a chemical compound that belongs to the carbazole family, which are heterocyclic organic compounds. It is composed of carbon, hydrogen, and oxygen atoms, and features functional groups such as methoxy groups and aromatic rings. Although its specific applications and properties are not extensively studied, carbazole compounds are known for their biological activities, including antimicrobial, antiviral, and anticancer properties, suggesting that 3,6-Dimethoxy-9H-carbazole could be utilized in similar medicinal or chemical applications.

3,6-Dimethoxy-9H-carbazole

Detailed Information

Product Name:3,6-Dimethoxy-9H-carbazole
CasNo.:57103-01-2
MF:C14H13NO2
MW:227.25900

pd_nature

Purity:99%
pd_boiling:131-133 °C
Packing:
Throughput:

Product Details;

CasNo： 57103-01-2

MF： C14H13NO2

Factory Sells Best Quality 3,6-Dimethoxy-9H-carbazole 57103-01-2 with steady supply

Molecular Formula:C14H13NO2
Molecular Weight:227.25900
Melting Point:131-133 °C
Boiling Point:426.7±25.0 °C(Predicted)
PKA:17.26±0.30(Predicted)
PSA：34.25000
Density:1.235±0.06 g/cm3(Predicted)
LogP:3.33830

57103-01-2 Relevant articles

Development of colloidally stable carbazole-based fluorescent nanoaggregates

Svechkarev, Denis,Kyrychenko, Alexander,Payne, William M.,Mohs, Aaron M.

, p. 55 - 64 (2018)

Fluorescent nanomaterials require high c...

Pyridazine–carbazole based fluorescent probes for volatile acid detection

Han, Won-Sik,Kim, Seung-Hwan,Lee, Sohee,Lee, Sunhee,Lee, Yeeun,Lee, Yong Sup,Wang, Kang-Kyun,Yang, Kwang-Hwan

, (2021)

Stimuli-responsive materials based on do...

Enhancement of redox stability and electrochromic performance of aromatic polyamides by incorporation of (3,6-dimethoxycarbazol-9-yl)-triphenylamine units

Wang, Hui-Min,Hsiao, Sheng-Huei

, p. 272 - 286 (2014)

New series aromatic polyamides with (car...

A star-shaped cyclopentadithiophene-based dopant-free hole-transport material for high-performance perovskite solar cells

Lee, Kun-Mu,Yang, Jui-Yu,Lai, Ping-Sheng,Luo, Ke-Jyun,Yang, Ting-Yu,Liau, Kang-Ling,Abate, Seid Yimer,Lin, Yan-Duo

, p. 6444 - 6447 (2021/07/02)

A new cyclopentadithiophene (CPDT)-based...

A simple strategy to achieve efficient thermally activated delayed fluorescent emitters via enhancing electron donating ability of donors

Li, Ganggang,Li, Jiafang,Li, Kai,Liu, He,Liu, Zhiwen,Wang, Zhiming,Yang, Chuluo,Zhan, Qun,Zhang, Bing,Zhou, Changjiang

, (2020/05/18)

Simultaneously achieving both effective ...

One-pot synthesis of a white-light emissive bichromophore operated by aggregation-induced dual emission (AIDE) and partial energy transfer

Biesen, Lukas,Deni?en, Melanie,Hannen, Ricarda,Hoffmann, Katrin,Itskalov, Dana,Müller, Thomas J. J.,Nirmalananthan-Budau, Nithiya,Reiss, Guido J.,Resch-Genger, Ute

supporting information, p. 7407 - 7410 (2020/07/15)

Merocyanine-triarylamine bichromophores ...

57103-01-2 Process route

: 67-56-1
methanol

: 6825-20-3
3,6-dibromo-9H-carbazole

: 57103-01-2
3,6-di-methoxy-9H-carbazole

Conditions

Conditions	Yield
methanol; With sodium; at 0 - 20 ℃; for 2h; Inert atmosphere; Schlenk technique; 3,6-dibromo-9H-carbazole; With copper(l) iodide; In N,N-dimethyl-formamide; at 80 ℃; for 24h; Inert atmosphere; Schlenk technique;	85%
With copper(l) iodide; sodium; In N,N-dimethyl-formamide; at 120 ℃; for 3h; Inert atmosphere;	62%
With copper(l) iodide; sodium methylate; In N,N-dimethyl-formamide; Inert atmosphere; Schlenk technique;	62%
With sodium methylate; copper(I) bromide; Reflux;
With copper(l) iodide; sodium methylate; In N,N-dimethyl-formamide;

: 67-56-1
methanol

: 6825-20-3
3,6-dibromo-9H-carbazole

: 124-41-4
sodium methylate

: 57103-01-2
3,6-di-methoxy-9H-carbazole