438219-37-5

Basic information

• Product Name: 4-(4-ISOBUTYLPHENYL)-5-METHYL-1,3-THIAZOL-2-AMINE
• Synonyms: 4-(4-ISOBUTYLPHENYL)-5-METHYL-1,3-THIAZOL-2-AMINE;[4-(4-isobutylphenyl)-5-methyl-thiazol-2-yl]amine;4-(4-isobutylphenyl)-5-methyl-2-thiazolamine;4-(4-isobutylphenyl)-5-methyl-thiazol-2-amine;5-methyl-4-[4-(2-methylpropyl)phenyl]-1,3-thiazol-2-amine;IVK/1011839;Oprea1_098924;ZINC00373353
• CAS NO: 438219-37-5
• Molecular Formula: C₁₄H₁₈N₂S
• Molecular Weight: 246.37112
• Mol File: 438219-37-5.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(4-ISOBUTYLPHENYL)-5-METHYL-1,3-THIAZOL-2-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-ISOBUTYLPHENYL)-5-METHYL-1,3-THIAZOL-2-AMINE(438219-37-5)
• EPA Substance Registry System: 4-(4-ISOBUTYLPHENYL)-5-METHYL-1,3-THIAZOL-2-AMINE(438219-37-5)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 438219-37-5(Hazardous Substances Data)

Upstream product

• 80336-66-9 2-chloro-1-(4-isobutyl-phenyl)1-propanone 
• 17356-08-0 thiourea 

Relevant articles and documents

Iridium-catalyzed 1,3-hydrogen shift/chlorination of allylic alcohols

Tandem: Allylic alcohols react with N-chlorosuccinimide (NCS) in a tandem 1,3-H shift/C-Cl bond formation leading to α-chloroketones and α-chloroaldehydes. The reactions proceed with complete selectivity to give single constitutional isomers of monochlorinated carbonyl compounds. The utility of the transformation is illustrated by the straightforward synthesis of 4,5-disubstituted 2-aminothiazoles from allylic alcohols. Copyright