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CAS

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61601-54-5

1-Hydroxycarbazole, also known as 3-hydroxycarbazole, is a chemical compound with the molecular formula C12H9NO. It is a white to light brown crystalline solid that is soluble in organic solvents but insoluble in water. 1-HYDROXYCARBAZOLE is recognized for its unique chemical structure and properties, making it a valuable component in various fields of research and industry. It is known to exhibit antioxidant and anti-inflammatory properties, which contribute to its potential applications in both medical and industrial sectors.

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  • 61601-54-5 Structure

  • Basic information

    1. Product Name: 1-HYDROXYCARBAZOLE
    2. Synonyms: 1-HYDROXYCARBAZOLE;9H-carbazol-1-ol
    3. CAS NO:61601-54-5
    4. Molecular Formula: C12H9NO
    5. Molecular Weight: 183.206
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 61601-54-5.mol

  • Chemical Properties

    1. Melting Point: 164 °C
    2. Boiling Point: 431.4°Cat760mmHg
    3. Flash Point: 214.7°C
    4. Appearance: /
    5. Density: 1.362g/cm3
    6. Vapor Pressure: 4.78E-08mmHg at 25°C
    7. Refractive Index: 1.815
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 10.10±0.30(Predicted)
    11. CAS DataBase Reference: 1-HYDROXYCARBAZOLE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 1-HYDROXYCARBAZOLE(61601-54-5)
    13. EPA Substance Registry System: 1-HYDROXYCARBAZOLE(61601-54-5)

  • 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: 61601-54-5(Hazardous Substances Data)

61601-54-5 Usage

Uses

Used in Pharmaceutical Synthesis:
1-Hydroxycarbazole is used as a building block in the synthesis of organic compounds and pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, potentially leading to advancements in medicinal chemistry.
Used in Optoelectronics:
1-Hydroxycarbazole has potential applications in the field of optoelectronics due to its specific chemical and physical properties. It can be utilized in the development of electronic devices that rely on the interaction of light with electronic components.
Used as a Corrosion Inhibitor:
In the industrial sector, 1-Hydroxycarbazole is used as a corrosion inhibitor. Its ability to protect materials from corrosion makes it a valuable asset in industries where metal protection is crucial, such as in the automotive, aerospace, and construction sectors.
Used in Antioxidant and Anti-Inflammatory Applications:
Due to its antioxidant and anti-inflammatory properties, 1-Hydroxycarbazole is used in medical applications to combat oxidative stress and inflammation, which are implicated in various diseases and conditions. This makes it a potential candidate for therapeutic interventions in healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 61601-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,0 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61601-54:
(7*6)+(6*1)+(5*6)+(4*0)+(3*1)+(2*5)+(1*4)=95
95 % 10 = 5
So 61601-54-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO/c14-11-7-3-5-9-8-4-1-2-6-10(8)13-12(9)11/h1-7,13-14H

61601-54-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 9H-Carbazol-1-ol

1.2 Other means of identification

Product number -
Other names hydroxy-pyridin-4-yl-methanesulfonic acid

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:61601-54-5 SDS

61601-54-5Relevant articles and documents

Alteration of the substrate specificity of the angular dioxygenase carbazole 1,9a-dioxygenase

Uchimura, Hiromasa,Horisaki, Tadafumi,Umeda, Takashi,Noguchi, Haruko,Usami, Yusuke,Li, Li,Terada, Tohru,Nakamura, Shugo,Shimizu, Kentaro,Takemura, Tetsuo,Habe, Hiroshi,Furihata, Kazuo,Omori, Toshio,Yamane, Hisakazu,Nojiri, Hideaki

body text, p. 3237 - 3248 (2009/04/10)

Carbazole 1,9a-dioxygenase (CARDO) consists of terminal oxygenase (CARDO-O) and electron transport components. CARDO can catalyze specific oxygenation for various substrates: angular dioxygenation for carbazole and dibenzo-p-dioxin, lateral dioxygenation for anthracene, and monooxygenation for methylene carbon of fluorene and sulfide sulfur of dibenzothiophene. To elucidate the molecular mechanism determining its unique substrate specificity, 17 CARDO-O site-directed mutants at amino acid residues I262, F275, Q282, and F329, which form the substrate-interacting wall around the iron active site by CARDO-O crystal structure, were generated and characterized. F329 replacement dramatically reduced oxygenation activity. However, several mutants produced different products from the wild-type enzyme to a large extent: I262V and Q282Y (1-hydroxycarbazole), F275W (4-hydroxyfluorene), F275A (unidentified cis-dihydrodiol of fluoranthene), and I262A and I262W (monohydroxydibenzothiophenes). These results suggest the possibility that the respective substrates bind to the active sites of CARDO-O mutants in a different orientation from that of the wild-type enzyme.

FLASH-VACUUM PYROLYSIS OF NITROARYLBENZOTRIAZOLES. A TANDEM MASS SPECTROMETRY STUDY

Maquestiau, Andre,Flammang-Barbieux, Monique,Flammang, Robert,Chen, Lin-Zhi

, p. 245 - 254 (2007/10/02)

Tandem mass spectrometry (MS/MS) has been applied to investigate the behaviour of 1-(2-nitrophenyl)benzotriazole upon flash-vacuum pyrolysis (FVP) conditions.Above 500 deg C, is pyrolyzed to give a mixture of 1-nitrocarbazole , 1-hydroxycarbazole and carbazole .Under similar conditions, 2-(2-nitrophenyl)benzotriazole appears to be more stable; it is however partially isomerized into 8 at high temperatures.Aza analogs of 8, like 1-(2-nitro-4-pyridyl)benzotriazole also loose nitrogen above 500 deg C to give a mixture of 1-nitro-3-azacarbazole , 1-hydroxy-3-azacarbazole and 3-azacarbazole .

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