1465-10-7 Usage
Uses
Used in Organic Synthesis:
L-Cystine, N,N'-bis[(4-methylphenyl)sulfonyl]is used as a reagent in organic synthesis for the introduction of sulfonyl groups into molecules. The presence of sulfonyl groups can significantly alter the properties and reactivity of the target molecules, making L-Cystine,N,N'-bis[(4-methylphenyl)sulfonyl]- a versatile tool in the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
L-Cystine, N,N'-bis[(4-methylphenyl)sulfonyl]is used as a building block in the pharmaceutical industry for the development of new drug candidates. The biological activities of sulfonyl groups, such as anti-inflammatory and antibacterial properties, make L-Cystine,N,N'-bis[(4-methylphenyl)sulfonyl]- a promising starting point for the design and synthesis of novel therapeutic agents. Additionally, the 4-methylphenyl groups can influence the compound's solubility and reactivity, allowing for the fine-tuning of drug properties and efficacy.
Used in Drug Design and Development:
L-Cystine, N,N'-bis[(4-methylphenyl)sulfonyl]is used in drug design and development to create new molecules with improved therapeutic effects. L-Cystine,N,N'-bis[(4-methylphenyl)sulfonyl]-'s unique structure and properties make it a valuable resource for medicinal chemists, who can leverage its sulfonyl and 4-methylphenyl groups to design drugs with enhanced potency, selectivity, and pharmacokinetic profiles. Further research on L-Cystine,N,N'-bis[(4-methylphenyl)sulfonyl]- could lead to the discovery of innovative treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 1465-10-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,6 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1465-10:
(6*1)+(5*4)+(4*6)+(3*5)+(2*1)+(1*0)=67
67 % 10 = 7
So 1465-10-7 is a valid CAS Registry Number.
1465-10-7Relevant academic research and scientific papers
Chen, Lin,Cui, Yu-Sheng,Duan, Xiu,Guo, Kai,Qin, Long-Zhou,Qiu, Jiang-Kai,Sun, Qi,Yuan, Xin,Zhuang, Kai-Qiang
, p. 5093 - 5104 (2020)
We describe the application of S?H bond insertion reactions of aryl diazoacetates with cysteine residues that enabled metal-free, S?H functionalization under visible-light conditions. Moreover, this process could be intensified by a continuous-flow photomicroreactor on the acceleration of the reaction (6.5 min residence time). The batch and flow protocols described were applied to obtain a wide range of functionalized cysteine derivatives and cysteine-containing dipeptides, thus providing a straightforward and general platform for their functionalizations in mild conditions. (Figure presented.).
