Alkylating agent nitrogen mustard compounds

Product Application：p-Cyanophenyl Isothiocyanate is an synthetic isothiocyanate derivative with potential anti-NF-kB and anti-inflammatory activities. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the

Product Application：p-Cyanophenyl Isothiocyanate is an synthetic isothiocyanate derivative with potential anti-NF-kB and anti-inflammatory activities. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the

Synonym(s): 4-Vinylbenzonitrile Formula: C9H7N Formula weight: 129.16 Purity: 97%, stab.

4-Methoxy-3-nitrobenzoic acid has been studied as a potential antitumor agent as an aniline mustard analog. 4-Methoxy-3-nitrobenzoic acid is also used as a starting reagent for the synthesis of BIPHEP-1-OMe, a precatalyst for the reaction of

4-Methoxy-3-nitrobenzoic acid has been studied as a potential antitumor agent as an aniline mustard analog. 4-Methoxy-3-nitrobenzoic acid is also used as a starting reagent for the synthesis of BIPHEP-1-OMe, a precatalyst for the reaction of

4-Methoxy-3-nitrobenzoic acid has been studied as a potential antitumor agent as an aniline mustard analog. 4-Methoxy-3-nitrobenzoic acid is also used as a starting reagent for the synthesis of BIPHEP-1-OMe, a precatalyst for the reaction of

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 0.

Application：Reactant or reagent involved in:Electrophilic cyclization of 2-alkynylanisoles or alkynylanilinesOxidative chlorination to sulfonyl chloridesArylation with triarylbismuthanesDecarboxylative cross-coupling with dialkoxybenzoic

Application：Reactant or reagent involved in:Electrophilic cyclization of 2-alkynylanisoles or alkynylanilinesOxidative chlorination to sulfonyl chloridesArylation with triarylbismuthanesDecarboxylative cross-coupling with dialkoxybenzoic

4-Phenyl-3-butyn-2-one is an α,β-ketoalkyne. Reaction of 4-phenyl-3-butyn-2-one with bromine chloride and iodine monochloride in CH2Cl2, CH2Cl2/pyridine and MeOH are studied.[1] Reduction of 4-phenyl-3-butyn-2-one in THF solution has been reported.

4-Phenyl-3-butyn-2-one is an α,β-ketoalkyne. Reaction of 4-phenyl-3-butyn-2-one with bromine chloride and iodine monochloride in CH2Cl2, CH2Cl2/pyridine and MeOH are studied.[1] Reduction of 4-phenyl-3-butyn-2-one in THF solution has been reported.

4-Phenyl-3-butyn-2-one is an α,β-ketoalkyne. Reaction of 4-phenyl-3-butyn-2-one with bromine chloride and iodine monochloride in CH2Cl2, CH2Cl2/pyridine and MeOH are studied.[1] Reduction of 4-phenyl-3-butyn-2-one in THF solution has been reported.