3D-CDA08907 - 4-ethenyloxyphenylmethanol
Benzenemethanol, 4-amino-3-methoxy-
CAS:Fórmula:C8H11NO2Pureza:96%Cor e Forma:SolidPeso molecular:153.17844-Hydroxy-3-Methoxybenzyl Alcohol
CAS:Fórmula:C8H10O3Pureza:95%Cor e Forma:SolidPeso molecular:154.16322-Methoxybenzenemethanol
CAS:Produto ControladoApplications 2-Methoxybenzenemethanol is used in the synthesis of antimycobacterial and antibacterial derivatives. Also used in the synthesis of phthalazines and analogues as benzodiazepine receptor ligands with specific activity.
References Wei, Z. et al.: Molecules., 18, 3872 (2013); Carling, R. et al.: J. Med. Chem., 47, 1807 (2004);Fórmula:C8H10O2Cor e Forma:NeatPeso molecular:138.16(2-Bromo-3-methylphenyl)methanol
CAS:The 2-bromo-3-methylphenylmethanol (BMPM) is a modulated phenyl ring with a stepwise, efficient biradical strategy. It has been shown to be photoresponsive and can undergo a photochemical reaction in the presence of photons. BMPM is an efficient organic compound that can be used for different strategies, such as a photochromic material for windows or solar cells. The change in color from white to yellow occurs when the molecule absorbs light in the visible spectrum. The color returns to its original state when it is irradiated with ultraviolet radiation.Fórmula:C8H9BrOPureza:Min. 95%Peso molecular:201.07 g/molN-[(3-Methoxyphenyl)methyl]hexadecanamide
CAS:N-[(3-Methoxyphenyl)methyl]hexadecanamide is a synthetic compound, which is a fatty acid amide derived from the reaction between 3-Methoxyphenylmethanol and hexadecanoic acid (palmitic acid). This compound is primarily synthesized in the laboratory through an amidation reaction, wherein the carboxylic acid group of palmitic acid reacts with the amino group of 3-Methoxyphenylmethanol. The result is a stable amide linkage.
Fórmula:C24H41NO2Pureza:Min. 95%Peso molecular:375.6 g/mol(±)-1-Phenylethyl Alcohol
CAS:Fórmula:C8H10OPureza:>98.0%(GC)Cor e Forma:White or Colorless to Almost white or Almost colorless powder to lump to clear liquidPeso molecular:122.17(+/-)-1-Phenylethanol, 97%
CAS:The Arthrobacter sp. is able to grow with (+ I-,(-)-1-phenylethanol or the racemic mixture as sole source of carbon. Growth is most rapid with the (-)-isomer, doubling time 12 h. Lipases show good activity and, in some cases, improved enantioselectivity when employed in pure ionic liquids for dynami
Fórmula:C8H10OPureza:97%Cor e Forma:Liquid, Clear colorlessPeso molecular:122.17Benzenemethanol, 3-bromo-5-methoxy-
CAS:Fórmula:C8H9BrO2Pureza:98%Cor e Forma:SolidPeso molecular:217.0599(4-Methoxy-3-(3-methoxypropoxy)phenyl)methanol
CAS:Fórmula:C12H18O4Pureza:%Cor e Forma:LiquidPeso molecular:226.26894-Methoxy-3-(3-Methoxypropoxy)Benzenemethanol
CAS:4-Methoxy-3-(3-Methoxypropoxy)BenzenemethanolPureza:98%Peso molecular:226.27g/mol3-Bromo-5-methoxybenzyl alcohol
CAS:3-Bromo-5-methoxybenzyl alcoholFórmula:C8H9BrO2Pureza:98%Cor e Forma: white to off-white solidPeso molecular:217.06g/molASTM Method D7845 Check Standard 0.01-0.05 Wt% in Toluene
CAS:Produto Controlado- 100-42-5
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- 1195-32-0
- 122-99-6
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- 2039-89-6
- 2234-20-0
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- 4169-04-4
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- 98-83-9
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- 99-89-8
Cor e Forma:Mixture5-Bromo-3-methoxybenzyl alcohol
CAS:5-Bromo-3-methoxybenzyl alcohol is a synthetic hydroxyphenyl compound that can be used as a coupling agent. It is prepared by the reaction of bromoacetaldehyde with 3-hydroxybenzyl alcohol in the presence of an amine base, such as pyridine. 5-Bromo-3-methoxybenzyl alcohol can also be used to synthesize pyridines and bromides.Fórmula:C8H9BrO2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:217.06 g/mol
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