77472-39-0

Usage

Uses

Used in Chemical Industry:
(3-NITROBENZYL)MERCAPTAN 97 is used as a reagent in organic synthesis for its ability to facilitate the production of a variety of organic compounds. Its unique properties make it a valuable component in the synthesis process.
Used in Pharmaceutical Industry:
(3-NITROBENZYL)MERCAPTAN 97 is used as a starting material for the synthesis of new drugs and other organic substances. Its versatility in chemical reactions contributes to the development of innovative pharmaceutical products.
Used in the Production of Sulfur-Containing Compounds:
(3-NITROBENZYL)MERCAPTAN 97 is utilized as a precursor in the synthesis of various sulfur-containing compounds, which have diverse applications across different industries, including the production of agrochemicals, dyes, and other specialty chemicals.

InChI:InChI=1/C7H7NO2S/c9-8(10)7-3-1-2-6(4-7)5-11/h1-4,11H,5H2

Upstream product

• 619-23-8 3-Nitrobenzyl chloride 
• 70102-34-0 3-nitrothiobenzamide 
• 66907-51-5 3-nitrobenzyl thiocyanate 
• 1335107-28-2 ethoxy(((3-nitrophenyl)methyl)sulfanyl)methanethione 
• 7647-01-0 hydrogenchloride 

Downstream Products

• 93533-35-8 1,2-bis(3-nitrobenzyl)disulfide 
• 51392-50-8 bis(3-nitrobenzyl)sulfane 
• 51392-54-2 1-[(methylsulfanyl)methyl]-3-nitrobenzene 
• 145872-60-2 2-(3-amino-phenylmethanesulfonyl)-ethanol 
• 90607-33-3 3-[(methylsulfanyl)methyl]aniline 
• 1039752-88-9 4-[(3-nitrobenzyl)thio]-7-(β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine 
• 1335107-30-6 (2,2,5-trimethyl-1,3-dioxan-5-yl)methyl (3-nitrophenyl)methanesulfonate 
• 1335107-31-7 (2,2,5-trimethyl-1,3-dioxan-5-yl)methyl (3-aminophenyl)methanesulfonate 
• 1335107-32-8 (2,2,5-trimethyl-1,3-dioxan-5-yl)methyl (3-hydrazinylphenyl)methanesulfonate 
• 1335107-33-9 C₅₁H₆₈N₄O₉S₄ 
• 58032-84-1 (3-nitrophenyl)methanesulfonyl chloride 
• 1458652-44-2 4-nitro-7-(3-nitrobenzylthio)benzo[c][1,2,5]oxadiazole 
• 1602769-44-7 N,N-dimethyl-7-(3-nitrobenzylthio)benzo[c][1,2,5]oxadiazole-4-sulfonamide 

Relevant academic research and scientific papers

Designed to dissolve: Suppression of colloidal aggregation of Cu(I)-selective fluorescent probes in aqueous buffer and in-gel detection of a metallochaperone

Due to the lipophilicity of the metal-ion receptor, previously reported Cu(I)-selective fluorescent probes form colloidal aggregates, as revealed by dynamic light scattering. To address this problem, we have developed a hydrophilic triarylpyrazoline-based fluorescent probe, CTAP-2, that dissolves directly in water and shows a rapid, reversible, and highly selective 65-fold fluorescence turn-on response to Cu(I) in aqueous solution. CTAP-2 proved to be sufficiently sensitive for direct in-gel detection of Cu(I) bound to the metallochaperone Atox1, demonstrating the potential for cation-selective fluorescent probes to serve as tools in metalloproteomics for identifying proteins with readily accessible metal-binding sites.

Correlation pKa - activitee catalitique des thiols dans la reeaction d'hydrolyse de l'aceetate de p-nitropheenyle

The kinetic study of the hydrolysis of p-nitrophenylacetate in the presence of primary thiols indicates the thiolate anion as the sole catalytic species.Comparison of the true second order constants (kRS-) reveals that purely aliphatic primary thiols behave differently from aromatic α-substituted primary thiols.In the latter group a correlation can be established between the true second order rate constants and the pKSH values by means of the Broensted equation log kRS- = βpKSH + C, with β equal to 0.40 and C equal to -0.85.