Similiar Molecules

• SMILES String: CCO
• Also know as: ethanol
• InChI=1/C2H6O/c1-2-3/h3H,2H2,1H3
• Molecular Formula: C2H6O
Reactions where this compound is a product:
• (Oxymercuration of alkenes)
0
from ethylene, water

• (Hydroboration of alkenes)
0
from ethylene, water

Reactions where this compound is a reactant:
• (Ester Formation from Carboxylic Acid)
0
with allyl hydrogen carbonateeth to form allyl ethyl carbonate

• with [(E)-3-phenylprop-2-enyl] hydrogen carbonateeth to form ethyl [(E)-3-phenylprop-2-enyl] carbonate
  
• with 2-oxo-3a,4,5,6,7,7a-hexahydro-3H-benzofuran-3-carboxylic acideth to form ethyl 2-oxo-3a,4,5,6,7,7a-hexahydro-3H-benzofuran-3-carboxylate
  
• with 2-acetoxycyclohex-3-ene-1-carboxylic acideth to form ethyl 2-acetoxycyclohex-3-ene-1-carboxylate
  
• with 4-methylene-5-oxo-tetrahydrofuran-3-carboxylic acideth to form ethyl 4-methylene-5-oxo-tetrahydrofuran-3-carboxylate
  
• with 2-oxooxazolidine-4-carboxylic acideth to form ethyl 2-oxooxazolidine-4-carboxylate
  
• with 2-allyloxycarbonylbenzoic acideth to form O2-allyl O1-ethyl benzene-1,2-dicarboxylate
  
• with 2-oxo-1-oxaspiro[4.5]decane-4-carboxylic acideth to form ethyl 2-oxo-1-oxaspiro[4.5]decane-4-carboxylate
  
• with 2-(2,2-dimethyl-5-oxo-tetrahydrofuran-3-yl)acetic acideth to form ethyl 2-(2,2-dimethyl-5-oxo-tetrahydrofuran-3-yl)acetate
  
• with eth to form
  
See all 105 reactions
• (Nucleophilic Acylation)
0
with 2-methyl-3-oxo-butanoyl chlorideeth to form ethyl 2-methyl-3-oxo-butanoate

• with 4-aminobenzoyl bromideeth to form ethyl 4-aminobenzoate
  
• with 4-aminobenzoyl chlorideeth to form ethyl 4-aminobenzoate
  
• with ethoxycarbonyl chloroformateeth to form ethoxycarbonyl ethyl carbonate
  
• with 2-amino-3-sulfanyl-propanoyl chlorideeth to form ethyl 2-amino-3-sulfanyl-propanoate
  
• with carbamoyl bromideeth to form ethyl carbamate
  
• with carbamoyl chlorideeth to form ethyl carbamate
  
• with carbamoyl fluorideeth to form ethyl carbamate
  
• with carbamoyl iodideeth to form ethyl carbamate
  
• with 2-hydroxy-2-methyl-propanoyl chlorideeth to form ethyl 2-hydroxy-2-methyl-propanoate
  
See all 3589 reactions
• (Sn2)
0
with 2-bromoethyl prop-2-enoateeth to form 2-ethoxyethyl prop-2-enoate

• with 2-chloroethyl prop-2-enoateeth to form 2-ethoxyethyl prop-2-enoate
  
• with 2-fluoroethyl prop-2-enoateeth to form 2-ethoxyethyl prop-2-enoate
  
• with 2-iodoethyl prop-2-enoateeth to form 2-ethoxyethyl prop-2-enoate
  
• with 1,2,2,2-tetrafluoroethanoleth to form 1-ethoxy-2,2,2-trifluoro-ethanol
  
• with 1,2,2,2-tetrachloroethanoleth to form 2,2,2-trichloro-1-ethoxy-ethanol
  
• with 3-bromoprop-1-eneeth to form 3-ethoxyprop-1-ene
  
• with 3-chloroprop-1-eneeth to form 3-ethoxyprop-1-ene
  
• with 3-fluoroprop-1-eneeth to form 3-ethoxyprop-1-ene
  
• with 3-iodoprop-1-eneeth to form 3-ethoxyprop-1-ene
  
See all 1863 reactions
• (Alkene formation via dehydration)
0
with e to form ethylene

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