
4-Methylphenylacetic acid | CAS:622-47-9
4-Methylphenylacetic acid
- Name:4-Methylphenylacetic acid
- CAS:622-47-9
- Synonyms:p-Tolylacetic Acid; p-Methylphenylacetic acid
- Molecular Formula:C9H10O2
- Molecular Weight:150.18
- EINESC:210-738-7
Description
Properties
Melting point | 90-93 ºC |
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Boiling point | 265-267 ºC |
Safety
SDS/MSDS | S24/25 |
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SDS
Source | SDS/MSDS Samples |
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Alfa-Aesar | View & Download |
Sigma-Aldrich | View & Download |
TCI | View & Download |
Synthetic Route
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More
Articles
Peer-Reviewed Papers
Characterization and inactivation of an agmatine deiminase from Helicobacter pylori.Justin E Jones et al.Bioorganic chemistry, 38(2), 62-73 (2009-12-29)
A mild liquid reduction route toward uniform blue-emitting EuCl2 nanoprisms and nanorods.Weili Jiang et al.Inorganic chemistry, 50(15), 6862-6864 (2011-06-28)
Gramicidin toxicity in NG108-15 cells: protective effects of acetamidine and guanidine.J A Doebler Cell biology and toxicology, 15(5), 279-289 (2000-05-17)
Synthesis of the sym-Triazine System. I. Trimerization and Cotrimerization of Amidines.Schaefer FC, et al. Journal of the American Chemical Society, 81(6), 1466-1470 (1959)
Selective inhibition of inducible nitric oxide synthase by derivatives of acetamidine.Cristina Maccallini et al.Medicinal chemistry (Shariqah (United Arab Emirates)), 8(6), 991-995 (2012-06-30)
Synthesis and antiparasitic activities of amidinic azolated derivatives.A Danan et al.Farmaco (Societa chimica italiana : 1989), 52(4), 227-229 (1997-04-01)
Four-component synthesis of fully substituted 1,2,4-triazoles.Steven T Staben et al.Angewandte Chemie (International ed. in English), 49(2), 325-328 (2009-12-10)
A synthesis of acetamidines.Jitendra R Harjani et al.The Journal of organic chemistry, 76(6), 1683-1691 (2011-02-15)
Chemical nature of the light emitter of the Aequorea green fluorescent protein.H Niwa et al.Proceedings of the National Academy of Sciences of the United States of America, 93(24), 13617-13622 (1996-11-26)
Differential effects of selective and non-selective inhibition of nitric oxide synthase on the expression and activity of cyclooxygenase-2 during gastric ulcer healing.Jin Sheng Guo et al.European journal of pharmacology, 536(3), 301-308 (2006-04-08)
Selective inhibition of iNOS by benzyl- and dibenzyl derivatives of N-(3-aminobenzyl)acetamidine.Marialuigia Fantacuzzi et al.ChemMedChem, 6(7), 1203-1206 (2011-05-14)
Novel aminobenzyl-acetamidine derivative modulate the differential regulation of NOSs in LPS induced inflammatory response: role of PI3K/Akt pathway.Antonia Patruno et al.Biochimica et biophysica acta, 1820(12), 2095-2104 (2012-09-07)
Gramicidin channel selectivity. Molecular mechanics calculations for formamidinium, guanidinium, and acetamidinium.B Turano et al.Biophysical journal, 63(1), 152-161 (1992-07-01)
Selectivity of externally facing ion-binding sites in the Na/K pump to alkali metals and organic cations.Ian M Ratheal et al.Proceedings of the National Academy of Sciences of the United States of America, 107(43), 18718-18723 (2010-10-13)
Small iminium ions block gramicidin channels in lipid bilayers.G Hemsley et al.Biophysical journal, 59(4), 901-907 (1991-04-01)
Isoguanosine substitution of conserved adenosines in the hammerhead ribozyme.M M Ng et al.Biochemistry, 33(40), 12119-12126 (1994-10-11)
Catalytic properties of human urinary kallikrein.E Antonini et al.Biochemistry, 21(10), 2477-2482 (1982-05-11)
Highly efficient copper-catalyzed cascade synthesis of quinazoline and quinazolinone derivatives.Cheng Huang et al.Chemical communications (Cambridge, England), (47)(47), 6333-6335 (2008-12-03)
Haloacetamidine-based inactivators of protein arginine deiminase 4 (PAD4): evidence that general acid catalysis promotes efficient inactivation.Bryan Knuckley et al.Chembiochem : a European journal of chemical biology, 11(2), 161-165 (2009-12-17)
Characterization of the synthetic compatible solute homoectoine as a potent PCR enhancer.Michael Schnoor et al.Biochemical and biophysical research communications, 322(3), 867-872 (2004-09-01)
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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