• Reaction of hydroxyquinazolinone with acetic anhydride and ethyl chloroacetate afforded (quinazolinyl)acetate and ethyl (quinazolinyloxy)acetate derivatives. (heterocycles.jp)
  • The quinazolinone reacted with benzoyl chloride, acetyl chloride and ethyl chloroacetate to afford N -(3-benzoyl-dihydroquinazolinyl) -N -phenylbenzamide, 3-acetylquinazolinone and ethyl quinazolinylacetate respectively. (heterocycles.jp)
  • Reaction of (2a-i) with ethyl chloroacetate followed by condensation with hydrazine hydrate yielded 2-[(4,6-disubstituted pyrimidine-2-yl) thio] acetohydrazides (4a-c). (ijpsonline.com)
  • German chemist Rudolf Fittig had tried to prepare a C-Zn nucleophile by reacting the metal with ethyl chloroacetate. (chemistryworld.com)
  • A detailed review and analysis was conducted of the biological effects of chloroacetic-acid (79118), sodium-chloroacetate (3926623), fluoroacetic-acid (144490), sodium-fluoroacetate (62748), iodoacetic-acid (64697), sodium- iodoacetate (305533), and bromoacetic-acid (79083). (cdc.gov)
  • Sodium chloroacetate is the organic compound with the formula CH2ClCO2Na. (wikipedia.org)
  • Sodium chloroacetate is a common laboratory reagent in organic chemistry as illustrated by many entries in the book series Organic Syntheses. (wikipedia.org)
  • With bifunctional nucleophiles, sodium chloroacetate is a precursor to heterocycles. (wikipedia.org)
  • The substance sodium chloroacetate completely dissociates (in water) into sodium and chloroacetate. (europa.eu)
  • While investigating the reactions of various carboxylic esters with organozinc reagents, Reformatskii had used methyl chloroacetate - which has chlorine attached adjacent to the carbonyl group. (chemistryworld.com)
  • Upon attempting to form diallylzinc in the same vessel, using Zaitsev's method, he found that zinc inserted into the carbon-chlorine bond of methyl chloroacetate instead of reacting with the allyl iodide. (chemistryworld.com)
  • Those cells were focally positive for naphthol AS-D chloroacetate esterase. (bvsalud.org)
  • The kinetics of the hydrolysis of benzaldehyde substituted (X) - phenyl methyl acetals and substituted (Y)-benzaldehyde phenyl methyl acetals were measured in pivalate , acetate, d1-deutero-acetate, beta-chloropropionate, formate and chloroacetate buffers, and in hydrochloric and deutero-chloric acids. (gla.ac.uk)
  • 2.04 in chloroacetate to -2.34 in pivalate, with a value of -1.94 for the hydronium ion catalysed reaction. (gla.ac.uk)
  • Methyl Chloroacetate, CAS No. 554-13-2, is a colorless to light yellow liquid with an intense pungent odor. (codchem.com)
  • Methyl Chloroacetate is primarily used as a intermediate in the synthesis of other chemicals. (codchem.com)
  • Methyl Chloroacetate can also be used as fluorinating agent, paint remover, and herbicide through in situ generation of phosgene. (codchem.com)
  • Sodium chloroacetate is the organic compound with the formula CH2ClCO2Na. (wikipedia.org)
  • Sodium chloroacetate is a common laboratory reagent in organic chemistry as illustrated by many entries in the book series Organic Syntheses. (wikipedia.org)
  • With bifunctional nucleophiles, sodium chloroacetate is a precursor to heterocycles. (wikipedia.org)
  • The mixture of the products contains sodium tri chloroacetate and another compound. (quiz-magic.com)
  • 3- Cyano pyridone derivatives were synthesized by treating 1-(4-bromophenyl)-3-(4-(dimethyl amino) phenyl) prop-2-en-1-one with compounds containing active methylene group in the presence of ammonium acetate. (tsijournals.com)
  • Herein, we propose a self-template synthesis strategy for preparing oxygen-rich porous carbons (ORC) by directly carbonizing potassium chloroacetate (ClCH2COOK) as the single carbon source. (edu.sa)
  • Chloroacetate is a good alkylating agent, serving as a reagent for affixing the -CH2CO2− group to a wide variety of even weak nucleophiles. (wikipedia.org)