141619-53-6

Basic information

• Product Name: 2-(2,4-Dichloro-phenyl)-2-(1-methyl-allyl)-oxirane
• CAS NO: 141619-53-6
• Molecular Weight: 243.133
• Mol File: 141619-53-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(2,4-Dichloro-phenyl)-2-(1-methyl-allyl)-oxirane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,4-Dichloro-phenyl)-2-(1-methyl-allyl)-oxirane(141619-53-6)
• EPA Substance Registry System: 2-(2,4-Dichloro-phenyl)-2-(1-methyl-allyl)-oxirane(141619-53-6)

Safety Data

• Hazardous Substances Data: 141619-53-6(Hazardous Substances Data)

Upstream product

• 591-97-9 1-chloro-2-butene 
• 4252-78-2 2,2',4'-trichloroacetophenone 

Downstream Products

• 126917-40-6 (2R^*,3S^*)-4-amino-2-(2,4-dichlorophenyl)-3-methyl-1-(1H-1,2,4-triazol-1-yl)-4-<4-(trifluoromethyl)benzoylamino>-2-butanol 
• 126917-41-7 (2R^*,3S^*)-4-<(E)-4-chlorocinnamoylamino>-2-(2,4-dichlorophenyl)-3-methyl-1-(1H-1,2,4-triazol-1-yl)-2-butanol 
• 126917-35-9 (2R^*,3R^*)-3-(2,4-dichlorophenyl)-2-methyl-4-(1H-1,2,4-triazol-1-yl)-1,3-butanediol 
• 126917-35-9 (2S^*,3R^*)-3-(2,4-dichlorophenyl)-2-methyl-4-(1H-1,2,4-triazol-1-yl)-1,3-butanediol 
• 126917-33-7 (2S^*,3R^*)-3-(2,4-dichlorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)butanol 
• 126917-33-7 (2R^*,3R^*)-3-(2,4-dichlorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)butanol 
• 126917-37-1 (2R^*,3S^*)-2-(2,4-dichlorophenyl)-4-methanesulfonyloxy-3-methyl-1-(1H-1,2,4-triazol-1-yl)-2-butanol 
• 126917-39-3 (2R^*,3S^*)-4-amino-2-(2,4-dichlorophenyl)-3-methyl-1-(1H-1,2,4-triazol-1-yl)-2-butanol 
• 95857-45-7 (2R^*,3S^*)-2-(2,4-dichlorophenyl)-3-methyl-1-(1H-1,2,4-triazol-1-yl)-4-penten-2-ol 
• 95857-45-7 (2R^*,3R^*)-2-(2,4-dichlorophenyl)-3-methyl-1-(1H-1,2,4-triazol-1-yl)-4-penten-2-ol 

Relevant articles and documents

Triazole antifungals. V. Synthesis and antifungal activities of some amides related to 3-acylamino-2-aryl-1-triazolyl-2-butanol

Amides, 2 and 3, related to the potent antifungal triazole-amide 3-acylamino-2-aryl-1-triazolyl-2-butanol (1) were synthesized starting from the triazole-alcohol 6. The antifungal activity of 2 and 3 against a mouse systemic Candida albicans infection was