2,4-dimethylaniline
Similiar Molecules
Click here to search for similiar molecules- SMILES String: CC1=CC(=C(C=C1)N)C
- Also know as: 2,4-dimethylaniline
- InChI=1/C8H11N/c1-6-3-4-8(9)7(2)5-6/h3-5H,9H2,1-2H3
- Molecular Formula: C8H11N
- Reactions where this compound is a reactant:
- (Amide Formation from an Acid Chloride) 0
- with 2-dimethylaminoacetyl chloride2,4-dimethylani to form 2-dimethylamino-N-(2,4-dimethylphenyl)acetamide
- with formyl chloride2,4-dimethylani to form N-(2,4-dimethylphenyl)formamide
- with 2-chloroacetyl chloride2,4-dimethylani to form 2-chloro-N-(2,4-dimethylphenyl)acetamide
- with isopropyl chloroformate2,4-dimethylani to form isopropyl N-(2,4-dimethylphenyl)carbamate
- with N-(4-methylphenyl)carbamoyl chloride2,4-dimethylani to form 1-(2,4-dimethylphenyl)-3-(4-methylphenyl)urea
- with N-isopropylcarbamoyl chloride2,4-dimethylani to form 3-(2,4-dimethylphenyl)-1-isopropyl-urea
- with N-ethylcarbamoyl chloride2,4-dimethylani to form 1-(2,4-dimethylphenyl)-3-ethyl-urea
- with N-propylcarbamoyl chloride2,4-dimethylani to form 1-(2,4-dimethylphenyl)-3-propyl-urea
- with 2-cyanoacetyl chloride2,4-dimethylani to form 2-cyano-N-(2,4-dimethylphenyl)acetamide
- (Amide Formation from a Carboxylic Acid) 0
- with 2-oxo-2-(sec-butylamino)acetic acid2,4-dimethylani to form N'-(2,4-dimethylphenyl)-N-sec-butyl-oxamide
- with cyclopropylcarbamic acid2,4-dimethylani to form 1-cyclopropyl-3-(2,4-dimethylphenyl)urea
- with 4-(N'-methoxycarbonylhydrazino)-4-oxo-butanoic acid2,4-dimethylani to form methyl N-[[4-[(2,4-dimethylphenyl)amino]-4-oxo-butanoyl]amino]carbamate
- with 2-(cyclohexylamino)-2-oxo-acetic acid2,4-dimethylani to form N-cyclohexyl-N'-(2,4-dimethylphenyl)oxamide
- with 2-(isopropylamino)-2-oxo-acetic acid2,4-dimethylani to form N'-(2,4-dimethylphenyl)-N-isopropyl-oxamide
- with (2-methylcyclohexyl)carbamic acid2,4-dimethylani to form 3-(2,4-dimethylphenyl)-1-(2-methylcyclohexyl)urea
- with (ethoxycarbonylamino)carbamic acid2,4-dimethylani to form ethyl N-[(2,4-dimethylphenyl)carbamoylamino]carbamate
- with 1-methylhexylcarbamic acid2,4-dimethylani to form 3-(2,4-dimethylphenyl)-1-(1-methylhexyl)urea
- with (1-ethyl-4-piperidyl)carbamic acid2,4-dimethylani to form 3-(2,4-dimethylphenyl)-1-(1-ethyl-4-piperidyl)urea
- (Nucleophilic Acylation) 0
- with acetyl chloride2,4-dimethylani to form N-(2,4-dimethylphenyl)acetamide
- with acetyl fluoride2,4-dimethylani to form N-(2,4-dimethylphenyl)acetamide
- with acetyl iodide2,4-dimethylani to form N-(2,4-dimethylphenyl)acetamide
- with 2-dimethylaminoacetyl chloride2,4-dimethylani to form 2-dimethylamino-N-(2,4-dimethylphenyl)acetamide
- with formyl bromide2,4-dimethylani to form N-(2,4-dimethylphenyl)formamide
- with formyl chloride2,4-dimethylani to form N-(2,4-dimethylphenyl)formamide
- with formyl fluoride2,4-dimethylani to form N-(2,4-dimethylphenyl)formamide
- with formyl iodide2,4-dimethylani to form N-(2,4-dimethylphenyl)formamide
- with 2-chloroacetyl bromide2,4-dimethylani to form 2-chloro-N-(2,4-dimethylphenyl)acetamide
- (Sn2) 0
- with 1-chloro-3-(isopropylamino)propan-2-ol2,4-dimethylani to form 1-[(2,4-dimethylphenyl)amino]-3-(isopropylamino)propan-2-ol
- with 5-bromo-3-methyl-thiazolidine-2,4-dione2,4-dimethylani to form 5-[(2,4-dimethylphenyl)amino]-3-methyl-thiazolidine-2,4-dione
- with 3-bromo-2-methyl-propanoic acid2,4-dimethylani to form 3-[(2,4-dimethylphenyl)amino]-2-methyl-propanoic acid
- with 3-chloro-2-methyl-propanoic acid2,4-dimethylani to form 3-[(2,4-dimethylphenyl)amino]-2-methyl-propanoic acid
- with 3-iodo-2-methyl-propanoic acid2,4-dimethylani to form 3-[(2,4-dimethylphenyl)amino]-2-methyl-propanoic acid
- with 3-bromoprop-1-ene2,4-dimethylani to form N-allyl-2,4-dimethyl-aniline
- with 3-chloroprop-1-ene2,4-dimethylani to form N-allyl-2,4-dimethyl-aniline
- with 3-fluoroprop-1-ene2,4-dimethylani to form N-allyl-2,4-dimethyl-aniline
- with 3-iodoprop-1-ene2,4-dimethylani to form N-allyl-2,4-dimethyl-aniline
- (Alkene Halogenation) 0
- (Friedel-Crafts acylation) 0
- (Electrophilic aromatic bromination) 0
- (Electrophilic aromatic iodination) 0
- (Electrophilic aromatic sulfonation) 0
- (Urea formation from Carbodiimide) 0
- with 2,4-dimethylaniline1-isocyanato-4-methyl-ben to form 1-(2,4-dimethylphenyl)-3-(4-methylphenyl)urea
- with 2,4-dimethylaniline2-isocyanatopro to form 3-(2,4-dimethylphenyl)-1-isopropyl-urea
- with 2,4-dimethylanilineisocyanatoet to form 1-(2,4-dimethylphenyl)-3-ethyl-urea
- with 2,4-dimethylaniline2-chloroacetyl isocya to form 2-chloro-N-[(2,4-dimethylphenyl)carbamoyl]acetamide
- with 2,4-dimethylaniline3-isocyanatoprop-1 to form 3-allyl-1-(2,4-dimethylphenyl)urea
- with 2,4-dimethylaniline1-chloro-2-isocyanato-et to form 3-(2-chloroethyl)-1-(2,4-dimethylphenyl)urea
- with 2,4-dimethylaniline1-ethoxy-2-isocyanato-et to form 1-(2,4-dimethylphenyl)-3-(2-ethoxyethyl)urea
- with 2,4-dimethylaniline1-(isocyanatomethyl)-2-methoxy-ben to form 1-(2,4-dimethylphenyl)-3-[(2-methoxyphenyl)methyl]urea
- with 2,4-dimethylanilineoxomethanone hydra to form 3-amino-1-(2,4-dimethylphenyl)urea
- More Info at PubChem
- More Info at ChemSpider
- with acetyl chloride2,4-dimethylani to form N-(2,4-dimethylphenyl)acetamide
- with isopropylcarbamic acid2,4-dimethylani to form 3-(2,4-dimethylphenyl)-1-isopropyl-urea
- with acetyl bromide2,4-dimethylani to form N-(2,4-dimethylphenyl)acetamide
- with 1-bromo-3-(isopropylamino)propan-2-ol2,4-dimethylani to form 1-[(2,4-dimethylphenyl)amino]-3-(isopropylamino)propan-2-ol
- with 2,4-dimethylaniline1-chloro-2-isocyanato-ben to form 3-(2-chlorophenyl)-1-(2,4-dimethylphenyl)urea
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