25126-19-6

Basic information

• Product Name: (1R,2R)-2-(2,2-dichloro-acetylamino)-1-phenyl-propane-1,3-diol
• Synonyms: (1R,2R)-2-(2,2-dichloro-acetylamino)-1-phenyl-propane-1,3-diol
• CAS NO: 25126-19-6
• Molecular Weight: 278.135
• Mol File: 25126-19-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1R,2R)-2-(2,2-dichloro-acetylamino)-1-phenyl-propane-1,3-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R)-2-(2,2-dichloro-acetylamino)-1-phenyl-propane-1,3-diol(25126-19-6)
• EPA Substance Registry System: (1R,2R)-2-(2,2-dichloro-acetylamino)-1-phenyl-propane-1,3-diol(25126-19-6)

Safety Data

• Hazardous Substances Data: 25126-19-6(Hazardous Substances Data)

Upstream product

• 116-54-1 dichloroacetic acid methyl ester 
• 46032-98-8 (1R,2R)-2-amino-1-phenylpropane-1,3-diol 
• 79-36-7 dichloroacethyl chloride 
• 3306-06-7 (+/-)-threo-2-amino-1-phenyl-1,3-propanediol 
• 513-96-2 3,3,3-trichloro-2-hydroxy-propionitrile 
• 3306-06-7 (1RS,2SR)-2-amino-1-phenyl-propane-1,3-diol 
• 3018-12-0 dichloroacetonitrile 
• 872302-03-9 dichloroacetyl-phosphorous acid diethyl ester 

Downstream Products

• 115082-34-3 dichloroacetic acid-[(5R)-4c-(4-nitro-phenyl)-2ξ-oxo-2λ⁴-[1,3,2]dioxathian-5r-ylamide] 
• 116081-46-0 (1R,2R)-2-(2,2-dichloro-acetylamino)-1-(4-nitro-phenyl)-3-nitryloxy-propan-1-ol 
• 97407-57-3 (1RS,2RS)-1,3-diacetoxy-2-(2,2-dichloro-acetylamino)-1-phenyl-propane 
• 97407-57-3 (1RS:2SR)-2-(C.C-dichloro-acetylamino)-1.3-diacetoxy-1-phenyl-propane 
• 10318-17-9 (1RS,2RS)-1,3-diacetoxy-2-(2,2-dichloro-acetylamino)-1-(4-nitro-phenyl)-propane 
• 10318-17-9 (1RS,2SR)-1,3-diacetoxy-2-(2,2-dichloro-acetylamino)-1-(4-nitro-phenyl)-propane 
• 56-75-7 2-(2,2-dichloroacetylamino)-1-(4-nitrophenyl)propane-1,3-diol 
• 119-62-0 (1RS,2SR)-2-amino-1-(4-nitro-phenyl)-propane-1,3-diol 
• 56-75-7 chlorampenicol 
• 33485-03-9 (1RS,2RS)-2-(2,2-dichloro-acetylamino)-1-(4-nitro-phenyl)-1,3-bis-nitryloxy-propane 

Relevant articles and documents

Oxidant controlled regio- and stereodivergent azidohydroxylation of alkenes via I2 catalysis

A novel, I2 catalyzed regio- and stereodivergent vicinal azidohydroxylation of alkenes leading to 1,2-azidoalcohols in high yields (up to 92%) and excellent dr (up to 98%) has been developed. This unprecedented transformation employs NaN3 and DMF as N- and O-nucleophiles respectively. The role of DMF as the O-source in the reaction has been unequivocally proven by 18O labelling studies.