185-11-5 Usage
Uses
Used in Organic Synthesis:
2-Thiaspiro[3.5]nonane is used as a key intermediate in the synthesis of various organic compounds due to its distinctive bicyclic structure and sulfur atom, which can be further modified or functionalized to produce a wide range of chemical products.
Used in Pharmaceutical Industry:
2-Thiaspiro[3.5]nonane is utilized as a building block in the development of new pharmaceuticals, leveraging its unique reactivity and structural features to create innovative drug candidates with potential therapeutic applications.
Used in Drug Development:
2-Thiaspiro[3.5]nonane serves as a valuable tool in drug development, where its unique structure can be exploited to design and synthesize new molecules with specific biological activities, contributing to the discovery of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 185-11-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,8 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 185-11:
(5*1)+(4*8)+(3*5)+(2*1)+(1*1)=55
55 % 10 = 5
So 185-11-5 is a valid CAS Registry Number.
185-11-5Relevant academic research and scientific papers
Diverse ring opening of thietanes and other cyclic sulfides: An electrophilic aryne activation approach
Zheng, Tianyu,Tan, Jiajing,Fan, Rong,Su, Shuaisong,Liu, Binbin,Tan, Chen,Xu, Kun
, p. 1303 - 1306 (2018/02/14)
Organosulfides are a common class of structure units in bioactive molecules and functional materials motivating continuous developments of efficient synthetic methods. Herein, we report an electrophilic aryne-activated ring opening protocol of one or two
The Reductive Acylation of Organic Disulfides with Aldehydes under Photochemical and Radical Conditions
Takagi, Makoto,Goto, Setsuo,Tazaki, Masato,Matsuda, Tsutomu
, p. 1982 - 1987 (2007/10/02)
The irradiation of organic disulfides in aldehyde solvents resulted in the reductive fission of the S-S linkage, giving an equimolar mixture of the corresponding thiol and thiol acylate in a good yield.The cyclic disulfides gave mono S-acylated dithiols.The reaction proceeded by means of the photo-initiated radical chain mechanism, and AIBN (azobisisobutyronitrile) effected the same reaction under thermal conditions.
