From Wikipedia, the free encyclopedia
Chemical compound
Methylketol or 2-methylindole is a mildly
toxic and slightly
flammable
organic compound which occurs as a white solid which turns brown over time.
[1]
[2] It has
chemical formula
C9
H9
N.
[3]
Methylketol is used as an intermediate for synthesizing
dyes,
[4]
pigments,
[5]
optical brighteners, and
pharmaceuticals.
[6]
See also
References
-
^ Brown, Daniel R.; Clark, Bryan W.; Garner, Lindsey V. T.; Di Giulio, Richard T. (June 2015).
"Zebrafish cardiotoxicity: the effects of CYP1A inhibition and AHR2 knockdown following exposure to weak aryl hydrocarbon receptor agonists". Environmental Science and Pollution Research International. 22 (11): 8329–8338.
doi:
10.1007/s11356-014-3969-2.
ISSN
1614-7499.
PMC
4442063.
PMID
25532870.
-
^ Brown, D. R.; Clark, B. W.; Garner, L. V. T.; Di Giulio, R. T. (October 2016).
"Embryonic cardiotoxicity of weak aryl hydrocarbon receptor agonists and CYP1A inhibitor fluoranthene in the Atlantic killifish (Fundulus heteroclitus)". Comparative Biochemistry and Physiology. Toxicology & Pharmacology. 188: 45–51.
doi:
10.1016/j.cbpc.2016.05.005.
ISSN
1532-0456.
PMID
27211013.
-
^ Parker, Amie; Lamata, Pilar; Viguri, Fernando; Rodríguez, Ricardo; López, José A.; Lahoz, Fernando J.; García-Orduña, Pilar; Carmona, Daniel (2020-10-12).
"Half-sandwich complexes of osmium containing guanidine-derived ligands". Dalton Transactions. 49 (39): 13601–13617.
doi:
10.1039/d0dt02713h.
hdl:
10261/233133.
ISSN
1477-9234.
PMID
32975256.
S2CID
221913494.
-
^ Casas-Catalán, María José; Doménech-Carbó, María Teresa (May 2005).
"Identification of natural dyes used in works of art by pyrolysis-gas chromatography/mass spectrometry combined with in situ trimethylsilylation". Analytical and Bioanalytical Chemistry. 382 (2): 259–268.
doi:
10.1007/s00216-005-3064-0.
ISSN
1618-2642.
PMID
15782338.
S2CID
44407380.
-
^ Shaki, Hanieh; Gharanjig, Kamaladin; Khosravi, Alireza (July 2015).
"Synthesis and investigation of antimicrobial activity and spectrophotometric and dyeing properties of some novel azo disperse dyes based on naphthalimides". Biotechnology Progress. 31 (4): 1086–1095.
doi:
10.1002/btpr.2107.
ISSN
1520-6033.
PMID
25967675.
S2CID
25349059.
-
^ Ozcan-Sezer, Senem; Ince, Elif; Akdemir, Atilla; Ceylan, Özlem Öztürk; Suzen, Sibel; Gurer-Orhan, Hande (May 2019).
"Aromatase inhibition by 2-methyl indole hydrazone derivatives evaluated via molecular docking and in vitro activity studies". Xenobiotica; the Fate of Foreign Compounds in Biological Systems. 49 (5): 549–556.
doi:
10.1080/00498254.2018.1482029.
ISSN
1366-5928.
PMID
29804490.
S2CID
44062839.