Similiar Molecules

• SMILES String: C=CCN(CC=C)C(=O)CCl
• Also know as: N,N-diallyl-2-chloro-acetamide
• InChI=1/C8H12ClNO/c1-3-5-10(6-4-2)8(11)7-9/h3-4H,1-2,5-7H2
• Molecular Formula: C8H12ClNO
Reactions where this compound is a product:
• (Amide Formation from an Acid Chloride)
0
from 2-chloroacetyl chloride, N-allylprop-2-en-1-amine

• (Nucleophilic Acylation)
0
from 2-chloroacetyl bromide, N-allylprop-2-en-1-amine

• from 2-chloroacetyl chloride, N-allylprop-2-en-1-amine
  
• from 2-chloroacetyl fluoride, N-allylprop-2-en-1-amine
  
• from 2-chloroacetyl iodide, N-allylprop-2-en-1-amine
  
• (Sn2)
0
from 3-bromoprop-1-ene, N-allyl-2-chloro-acetamide

• from 3-chloroprop-1-ene, N-allyl-2-chloro-acetamide
  
• from 3-fluoroprop-1-ene, N-allyl-2-chloro-acetamide
  
• from 3-iodoprop-1-ene, N-allyl-2-chloro-acetamide
  
Reactions where this compound is a reactant:
• (Sn2)
0
with N,N-diallyl-2-chloro-acetamideisoindoline-1,3-d to form N,N-diallyl-2-(1,3-dioxoisoindolin-2-yl)acetamide

• with N,N-diallyl-2-chloro-acetamideph to form N,N-diallyl-2-(phenoxy)acetamide
  
• with N,N-diallyl-2-chloro-acetamide1-methylimidazolidine-2,4-d to form N,N-diallyl-2-(3-methyl-2,5-dioxo-imidazolidin-1-yl)acetamide
  
• with N,N-diallyl-2-chloro-acetamideeth to form N,N-diallyl-2-ethoxy-acetamide
  
• with N,N-diallyl-2-chloro-acetamide4-hydroxybenza to form 4-[2-(diallylamino)-2-oxo-ethoxy]benzamide
  
• with N,N-diallyl-2-chloro-acetamide5-amino-3-methyl-isoxazole-4-carboxylic to form [2-(diallylamino)-2-oxo-ethyl] 5-amino-3-methyl-isoxazole-4-carboxylate
  
• with N,N-diallyl-2-chloro-acetamide4,5,6,7-tetrahydrobenzothiophene-3-carboxylic to form [2-(diallylamino)-2-oxo-ethyl] 4,5,6,7-tetrahydrobenzothiophene-3-carboxylate
  
• with N,N-diallyl-2-chloro-acetamide1,3-diazaspiro[4.5]decane-2,4-d to form N,N-diallyl-2-(2,4-dioxo-1,3-diazaspiro[4.5]decan-3-yl)acetamide
  
• with N,N-diallyl-2-chloro-acetamidew to form N,N-diallyl-2-hydroxy-acetamide
  
• with N,N-diallyl-2-chloro-acetamidepipera to form N,N-diallyl-2-piperazin-1-yl-acetamide
  
See all 28 reactions
• (Enolate Substitution)
0
with acetic acidN,N-diallyl-2-chloro-aceta to form 4-(diallylamino)-4-oxo-butanoic acid

• with N,N-diallyl-2-chloro-acetamidebromomet to form N,N-diallyl-2-chloro-propanamide
  
• with N,N-diallyl-2-chloro-acetamidechloromet to form N,N-diallyl-2-chloro-propanamide
  
• with N,N-diallyl-2-chloro-acetamideiodomet to form N,N-diallyl-2-chloro-propanamide
  
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