221038-07-9

Basic information

• Product Name: 1-(chloromethyl)-2-isocyanato-3-methylbenzene
• CAS NO: 221038-07-9
• Molecular Weight: 181.622
• Mol File: 221038-07-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(chloromethyl)-2-isocyanato-3-methylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(chloromethyl)-2-isocyanato-3-methylbenzene(221038-07-9)
• EPA Substance Registry System: 1-(chloromethyl)-2-isocyanato-3-methylbenzene(221038-07-9)

Safety Data

• Hazardous Substances Data: 221038-07-9(Hazardous Substances Data)

Upstream product

• 87-62-7 2,6-dimethylaniline 
• 28556-81-2 2,6-dimethylphenylisocyanate 

Downstream Products

• 221038-11-5 4-[2-[(bromosulfonyl)methyl]-6-methylphenyl]-2,4-dihydro-5-methoxy-2-methyl-3H-1,2,4-triazol-3-one 
• 185686-21-9 4-[2-(bromomethyl)-6-methylphenyl]-2,4-dihydro-5-methoxy-2-methyl-3H-1,2,4-triazol-3-one 
• 221038-13-7 2,4-dihydro-4-[2-(hydroxymethyl)-6-methylphenyl]-5-methoxy-2-methyl-3H-1,2,4-triazol-3-one 
• 221038-08-0 5-chloro-4-[2-(chloromethyl)-6-methylphenyl]-2,4-dihydro-2-methyl-3H-1,2,4-triazol-3-one 

Relevant articles and documents

Synthesis and properties of axially-chiral N-(2,6-disubstituted)phenyl triazolones

Certain ortho-substituted phenyl triazolone compounds are fungicidal. When two ortho-substituents are present, stable atropisomers can be isolated. Several methods for resolving racemic intermediates into the enantiomers are described, including separations of diasteromeric ester derivatives and diasteromeric salts. The intermediates were converted into products in which the absolute configuration can be correlated to biological activity.