Nimustine hydrochloride

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Application 4-Nitrobenzenesulfonyl chloride was used in the synthesis of [Cu(bipy)2Cl](nbs) where bipy = 2,2&#8242-bipyridine, nbs = 4-nitrobenzenesulfonate . It was also used to determine estrogens in biological fluids .

Application 4-Nitrobenzenesulfonyl chloride was used in the synthesis of [Cu(bipy) 2 Cl](nbs) (1) (bipy = 2,2&#8242-bipyridine, nbs = 4-nitrobenzenesulfonate) hydroxylamines of sulfadiazine and sulfamethoxazole solution phase peptide using N

Application 4-Nitrobenzenesulfonyl chloride was used in the synthesis of [Cu(bipy) 2 Cl](nbs) (1) (bipy = 2,2&#8242-bipyridine, nbs = 4-nitrobenzenesulfonate) hydroxylamines of sulfadiazine and sulfamethoxazole solution phase peptide using N

Application 4-Nitrobenzenesulfonyl chloride was used in the synthesis of [Cu(bipy) 2 Cl](nbs) (1) (bipy = 2,2&#8242-bipyridine, nbs = 4-nitrobenzenesulfonate) hydroxylamines of sulfadiazine and sulfamethoxazole solution phase peptide using N

4-Nitrobenzoyl chloride reacts with triphenylphosphonium salt to synthesize benzofurans (potential positron emission tomography (PET) tracers) by the intramolecular Wittig reaction .It has been used for the derivatisation of Adiol (Androstenediol,

4-Nitrobenzoyl chloride reacts with triphenylphosphonium salt to synthesize benzofurans (potential positron emission tomography (PET) tracers) by the intramolecular Wittig reaction .It has been used for the derivatisation of Adiol (Androstenediol,

4-Nitrobenzoyl chloride reacts with triphenylphosphonium salt to synthesize benzofurans (potential positron emission tomography (PET) tracers) by the intramolecular Wittig reaction .It has been used for the derivatisation of Adiol (Androstenediol,

4-Nitrobenzoyl chloride is a derivatization reagent. It reacts with L-glutamic acid undergoing methylation using formaldehyde, synthesizing N-(4-methylaminobenzoyl)glutaminic acid.

4-Nitrobenzyl chloride acts as substrate for glutathione S-transferase(GST) in determination of GST in Chinese fetal liver . It undergoes reduction by NADPH to yield 4-nitrotoluene .

4-Nitrobenzyl chloride acts as substrate for glutathione S-transferase(GST) in determination of GST in Chinese fetal liver . It undergoes reduction by NADPH to yield 4-nitrotoluene .

Application L-Glutamic acid &#947-(p-nitroanilide) hydrochloride has been used as a solute carrier family 1 member 5 (SLC1A5) inhibitor: or an inhibitor of the cell membrane glutamine transporter to study the effects of blocking glutamine uptake