Antidepressants

Analysis Note Assay (GC, area%): &#8805 99.0 % (a/a) Melting range (lower value): &#8805 119 &#176C Melting range (upper value): &#8804 122 &#176C Identity (IR): passes test

Application 2-Nitro-1-naphthol was employed as substrate for use in an amperometric 3-electrode system for the determination of alkaline phosphatase, the enzyme label most commonly used in electrochemical immunoassays. It was also used in the

2-Nitro-1h-indene-1，3(2h)-dione.

2-Nitro-1h-indene-1，3(2h)-dione.

2-Nitro-2'，4-dichlorodiphenyl ether.

2-Nitro-2'，4-dichlorodiphenyl ether.

2-Nitro-2'，4-dichlorodiphenyl ether.

2-Nitro-5-(propylthio)aniline.

Application Reactant involved in synthesis of: Cyclic nitrogen compounds via intramolecular hydroamination Pentacyclic lycopodium alkaloid huperzine-Q Pyrrolidines Intermolecular C-H insertion reactions Reactant involved in intermolecular amination

Application Reactant involved in synthesis of: Cyclic nitrogen compounds via intramolecular hydroamination Pentacyclic lycopodium alkaloid huperzine-Q Pyrrolidines Intermolecular C-H insertion reactions Reactant involved in intermolecular amination

Application 2-Nitrobenzyl bromide was used for caging unprotected cysteine-containing or thiophosphorylated peptides in aqueous solution . It can be used in the synthesis of ( R )- and ( S )-3-amino-3,4-dihydro-1 H -quinolin-2-one .

Application 2-Nitrobenzyl bromide was used for caging unprotected cysteine-containing or thiophosphorylated peptides in aqueous solution . It can be used in the synthesis of ( R )- and ( S )-3-amino-3,4-dihydro-1 H -quinolin-2-one .