While stirring the mixture, add a stoichiometric amount of Oxone to the reaction mixture. The Oxone will generate active halogen species in situ. The reaction should be performed at a low temperature (0-10°C) to control the reaction and prevent side reactions. You can use an ice bath or a low-temperature environment for this purpose.
If you need to purchase chemical raw materials, submit your demand information to get the latest quotations.
4H-1-Benzopyran-4-one, 3-iodo-2-(4-methoxyphenyl)-
METHANOL
Thiazolo[3,2-b][1,2,4]triazole-5-carboxylic acid, 6-(hydroxymethyl)-2-phenyl-, ethyl ester
TVB-2640
4-fluoroestradiol
C44H38F8N2P2
3
4
Methyl 4-amino-3-(benzyloxy)benzoate
2,4-dinitro-2,4-bis(phenylsulfonyl)butan-1-ol
3-methyl-3-((4-methylphenyl)sulfonyl)cyclopentanone
1,3-Dimethyl-8-piperidin-1-yl-7-{2-[piperidin-(2Z)-ylideneamino]-ethyl}-3,7-dihydro-purine-2,6-dione
2-(5-benzoyl-2-thienyl)naphtho[1,2-d]oxazole
5
2H-1,4-Benzothiazin-3(4H)-one, 2-[(acetyloxy)phenylmethyl]-2-hydroxy-4-methyl-
4-Nitro-benzoic acid (S)-2-phenoxy-1-(3-trimethylsilanyl-oxiranyl)-ethyl ester
methyl(2-((2-(phenylethynyl)phenyl)ethynyl)phenyl)sulfane
1-(2-(2-(but-3-enyl)-2-phenylcyclopropylidene)-1-phenylvinyl)benzene
1H-Pyrazole, 1-hydroxy-3,5-dimethyl-
2(1H)-Quinolinone, 6,7-dichloro-4-hydroxy-3-phenyl-
2-Chlor-phenylessigsaeure-N-<2-(3,4-dimethoxyphenyl)-ethylamid>
5-(2-phenylethenyl)-1,3,4-oxadiazol-2(3H)-one
N-[(Z)-1-Butylcarbamoyl-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-vinyl]-benzamide
Z-1-METHOXY-3,3,3-TRIFLUOROPROPENE
RHENIUM PENTACARBONYL CHLORIDE
methyl (4-amino-3,5-dibromophenyl)acetate
methyl 4,6-O-benzylidene-α-D-galactopyranoside 2-O-benzoate
N1-(4-IODO-2-METHYLPHENYL)ACETAMIDE
N-(2-bromophenyl)-N-methylnitrous amide
2-Amino-3-hydroxybenzaldehyde
7-keto dehydroabietic acid methyl ester
