Melting point	98-101 ºC

Symbol(GHS)	Xi
Hazard Codes	R36/37/38
SDS/MSDS	S26;S36

Source	SDS/MSDS Samples
没有数据	没有数据

Synthetic Route

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Name	CAS

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Articles

Peer-Reviewed Papers

Metabolism and pneumotoxicity of 3-methyloxindole, indole-3-carbinol, and 3-methylindole in goats.M J Potchoiba et al.American journal of veterinary research, 43(8), 1418-1423 (1982-08-01) Direct asymmetric anti-Mannich-type reactions catalyzed by cinchona alkaloid derivatives.Ying Jin et al.Chirality, 26(12), 801-805 (2014-07-22) Unbiased high-throughput screening of reactive metabolites on the linear ion trap mass spectrometer using polarity switch and mass tag triggered data-dependent acquisition.Zhengyin Yan et al.Analytical chemistry, 80(16), 6410-6422 (2008-07-23) Production of Indole-3-Lactic Acid by Bifidobacterium Strains Isolated fromHuman Infants.Takuma Sakurai et al.Microorganisms, 7(9) (2019-09-14) Facile and Efficient Enantioselective Hydroxyamination Reaction: Synthesis of 3-Hydroxyamino-2-Oxindoles Using Nitrosoarenes.Shen K, et al. Angewandte Chemie (Weinheim an der Bergstrasse, Germany), 123(20), 4780-4784 (2011) Porcine CYP2A19, CYP2E1 and CYP1A2 forms are responsible for skatole biotransformation in the reconstituted system.Jaroslav Matal et al.Neuro endocrinology letters, 30 Suppl 1, 36-40 (2009-12-23) Metabolism of 3-methylindole by vaccinia-expressed P450 enzymes: correlation of 3-methyleneindolenine formation and protein-binding.J Thornton-Manning et al.The Journal of pharmacology and experimental therapeutics, 276(1), 21-29 (1996-01-01)

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