
4-Methyl-3-methoxybenzonitrile | CAS:3556-60-3
4-Methyl-3-methoxybenzonitrile
- Name:4-Methyl-3-methoxybenzonitrile
- CAS:3556-60-3
- Synonyms:
- Molecular Formula:C9H9NO
- Molecular Weight:147.17
- EINESC:
Description
Properties
Melting point | 51-52.5 ºC** |
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Boiling point | 247.2±28.0 ºC (760 Tor |
Flash point | 102.9±17.9 ºC, 计算值* |
Density | 1.06±0.1 g/cm3 (20 ºC |
Safety
没有数据 | 没有数据 |
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SDS
Source | SDS/MSDS Samples |
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没有数据 | 没有数据 |
Synthetic Route
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More
Articles
Peer-Reviewed Papers
Inhibition of copper amine oxidase by haloamines: a killer product mechanism.R Medda et al.Biochemistry, 36(9), 2595-2602 (1997-03-04)
Enhanced Photodynamic Cancer Treatment by Mitochondria-Targeting and Brominated Near-Infrared Fluorophores.Ilkoo Noh et al.Advanced science (Weinheim, Baden-Wurttemberg, Germany), 5(3), 1700481-1700481 (2018-03-30)
Thrombolytic therapy based on fucoidan-functionalized polymer nanoparticles targeting P-selectin.Maya Juenet et al.Biomaterials, 156, 204-216 (2017-12-08)
Direct Pore Binding as a Mechanism for Isoflurane Inhibition of the Pentameric Ligand-gated Ion Channel ELIC.Qiang Chen et al.Scientific reports, 5, 13833-13833 (2015-09-09)
Quantitation of cysteine residues alkylated with 3-bromopropylamine by amino acid analysis.J E Hale et al.Analytical biochemistry, 216(1), 61-66 (1994-01-01)
Antagonist analogue of 6-[3 `-(1-adamantyl)-4 `-hydroxyphenyl]-2-naphthalenecarboxylic acid (AHPN) family of apoptosis inducers that effectively blocks AHPN-induced apoptosis but not cell-cycle arrest.Dawson M I, et al. Journal of Medicinal Chemistry, 47(14), 3518-3536 (2004)
Rational design of ligands targeting triplet repeating transcripts that cause RNA dominant disease: application to myotonic muscular dystrophy type 1 and spinocerebellar ataxia type 3.Alexei Pushechnikov et al.Journal of the American Chemical Society, 131(28), 9767-9779 (2009-06-26)
Identification of cysteine residues alkylated with 3-bromopropylamine by protein sequence analysis.R A Jue et al.Analytical biochemistry, 210(1), 39-44 (1993-04-01)
Optimization of the indenone ring of indenoisoquinoline topoisomerase I inhibitors.Morrell A, et al. Journal of Medicinal Chemistry, 50(18), 4388-4404 (2007)
Pharmaceutical micelles featured with singlet oxygen-responsive cargo release and mitochondrial targeting for enhanced photodynamic therapy.Xin Zhang et al.Nanotechnology, 29(25), 255101-255101 (2018-04-06)
On-line procedures for alkylation of cysteine residues with 3-bromopropylamine prior to protein sequence analysis.R A Jue et al.Analytical biochemistry, 221(2), 374-378 (1994-09-01)
Inhibition of tissue-bound semicarbazide-sensitive amine oxidase by two haloamines, 2-bromoethylamine and 3-bromopropylamine.H Kinemuchi et al.Archives of biochemistry and biophysics, 385(1), 154-161 (2001-05-22)
Interlocked host anion recognition by an indolocarbazole-containing [2] rotaxane.Brown A, et al. Journal of the American Chemical Society, 131(13), 4937-4952 (2009)
Synthesis and anticancer activity of simplified indenoisoquinoline topoisomerase I inhibitors lacking substituents on the aromatic rings.Nagarajan M, et al. Journal of Medicinal Chemistry, 47(23), 5651-5661 (2004)
A multi-mode-driven molecular shuttle: photochemically and thermally reactive azobenzene rotaxanes.Murakami H, et al. Journal of the American Chemical Society, 127(45), 15891-15899 (2005)
Mechanism of parkin activation by PINK1.Christina Gladkova et al.Nature, 559(7714), 410-414 (2018-07-12)
A 1,8-naphthalimide-based turn-on fluorescent probe for imaging mitochondrial hydrogen peroxide in living cells.Fang Dai et al.Free radical research, 52(11-12), 1288-1295 (2018-08-22)
Modification of cysteine.M W Crankshaw et al.Current protocols in protein science, Chapter 15, Unit15-Unit15 (2008-04-23)
Remarks
Products protected by valid patents are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1).
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