70164-13-5 Usage
Uses
Used in Coordination Chemistry:
2-(butylsulfanyl)-1,3,2-dithiaphospholane is used as a ligand for forming complexes with transition metal ions, which is crucial in the study and application of coordination chemistry.
Used in Organic Synthesis as a Catalyst:
In the field of organic synthesis, 2-(butylsulfanyl)-1,3,2-dithiaphospholane is utilized as a catalyst, contributing to the efficiency and selectivity of various chemical reactions, particularly in the production of fine chemicals and pharmaceuticals.
Used in Polymer Industry as a Stabilizer:
2-(butylsulfanyl)-1,3,2-dithiaphospholane serves as a stabilizer in the manufacture of polymers, enhancing the durability and performance of the final polymer products.
Used in Inorganic Chemistry Research:
Due to its unique molecular structure and reactivity, 2-(butylsulfanyl)-1,3,2-dithiaphospholane is an interesting subject of study for researchers in inorganic chemistry, potentially leading to new insights and applications in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 70164-13-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,6 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70164-13:
(7*7)+(6*0)+(5*1)+(4*6)+(3*4)+(2*1)+(1*3)=95
95 % 10 = 5
So 70164-13-5 is a valid CAS Registry Number.
70164-13-5Relevant academic research and scientific papers
PREPARATION AND STRUCTURAL STUDIES OF A NUMBER OF HETEROCYCLIC PHOSPHORANES
Denney, Donald B.,Denney, Dorothy Z.,Liu, Lun-Tsu
, p. 71 - 84 (2007/10/02)
A series monocyclic five-membered ring containing trivalent phosphorous compound with oxygen, nitrogen and sulfur bonded to phosphorous, in various combinations has been allowed to react with trifluoroethyl and 1,1,1,3,3,3-hexafluoroisopropyl benzenesulfenates.In some cases, pentacoordinated phosphorous compounds resulted.These materials have been studied by various NMR techniques.The same trivalent phosphorous compounds were allowed to react with 3,4-(bistrifluoromethyl)1,2,dithiete.In some cases phosphoranes were formed and they were also studied by NMR.
Cyclic dithiophospites
-
, (2008/06/13)
Compounds of the formula STR1 wherein R is an alkylene diradical of 2 to 3 carbon atoms, X is oxygen or sulfur, and R' is a hydrocarbyl group possessing herbicidal activity.
