38508-64-4

Upstream product

• 612-23-7 2-nitrobenzyl chloride 
• 7647-01-0 hydrogenchloride 
• 3958-60-9 2-nitrophenylmethyl bromide 
• 85071-27-8 2-nitrobenzyl thiocyanate 
• 81630-11-7 S-(2-nitrobenzyl)isothiourea hydrochloride 

Downstream Products

• 1437291-17-2 C₁₇H₁₈N₂O₄S₂ 
• 1437291-21-8 C₁₉H₂₀N₂O₄S₂ 
• 1437291-25-2 C₂₀H₂₂N₂O₄S₂ 
• 1437291-29-6 C₂₁H₂₄N₂O₆S₂ 
• 1437291-37-6 C₂₃H₂₂N₂O₅S₂ 
• 1437291-41-2 C₂₂H₁₉N₃O₆S₂ 
• 99366-73-1 1-nitro-3-{[(3-nitrophenyl)methane]sulfanylmethyl}benzene 
• 75663-55-7 4-(2-fluorophenyl)-1,2,3,6-tetrahydro-1-methylpyridine 
• 120034-00-6 (5S,6S)-6-(2-Nitro-benzylsulfanyl)-5,6-dihydro-benzo[c]phenanthren-5-ol 
• 120033-99-0 (5S,6S)-5-(2-Nitro-benzylsulfanyl)-5,6-dihydro-benzo[c]phenanthren-6-ol 

Relevant academic research and scientific papers

Prosthetic group linking arm, method for synthesizing same and method for synthesizing di-ubiquitin

The invention provides a process for synthesizing a prosthetic group linking arm and a method for synthesizing di-ubiquitin by the aid of the prosthetic group linking arm. The prosthetic group linkingarm, the process and the method have the advantages that the prosthetic group linking arm is easy to synthesize and store and stable in chemical property; the prosthetic group linking arm is high inchemical linking efficiency in procedures for synthesizing the di-ubiquitin by the aid of the novel prosthetic group linking arm, and protein linking can be carried out under physiological conditions;the novel prosthetic group linking arm can be removed under mild conditions, and accordingly harsh non-denaturation conditions in prosthetic group removal procedures for chemical synthetic protein ubiquitination at present can be omitted.

Synthesis of a photocontrollable hydrogen sulfide donor using ketoprofenate photocages

We report the design, synthesis and application of a directly photocontrollable hydrogen sulfide (H2S) donor, which releases H 2S proportionally to the intensity and duration of photoirradiation. Photocontrolled H2S releas

Light-induced hydrogen sulfide release from "caged" gem-dithiols

"Caged" gem-dithiol derivatives that release H2S upon light stimulation have been developed. This new class of H2S donors was proven, by various spectroscopic methods, to generate H2S in an aqueous/organic medium as well a

A novel C-5′ substituted cinchona alkaloid-derived catalyst promotes additions of alkyl thiols to nitroolefins with excellent enantioselectivity

A new bifunctional C-5′ substituted cinchona alkaloid-based catalyst promotes the first highly enantioselective additions of alkyl thiols to nitrostyrenes. The Royal Society of Chemistry 2012.

Probing the mechanism of electron capture and electron transfer dissociation using tags with variable electron affinity

Electron capture dissociation (ECD) and electron transfer dissociation (ETD) of doubly protonated electron affinity (EA)-tuned peptides were studied to further illuminate the mechanism of these processes. The model peptide FQpSEEQQQTEDELQDK, containing a