870708-65-9 Usage
Uses
Used in Pharmaceutical Research:
1-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-yl)thiourea is used as a key component in the development of new pharmaceuticals due to its unique structure and reactivity. Its potential applications in this field are vast and warrant further research and development.
Used in Material Science:
In the field of material science, 1-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-yl)thiourea is utilized as a building block for the creation of new materials and chemicals. Its distinctive bicyclic structure and thiourea functional group contribute to the development of innovative materials with potential applications in various industries.
Used in Organic Chemistry:
1-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-yl)thiourea is employed as a crucial intermediate in organic chemistry, facilitating the synthesis of a wide range of organic compounds. Its unique properties make it an essential tool for chemists working on the development of novel organic molecules.
It is important to handle 1-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-yl)thiourea with care and follow proper safety protocols when working with it in a laboratory setting, as with any chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 870708-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,7,0 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 870708-65:
(8*8)+(7*7)+(6*0)+(5*7)+(4*0)+(3*8)+(2*6)+(1*5)=189
189 % 10 = 9
So 870708-65-9 is a valid CAS Registry Number.
870708-65-9Relevant academic research and scientific papers
Caille, Seb,Boni, Jerome,Cox, Geoffrey B.,Faul, Margaret M.,Franco, Pilar,Khattabi, Saab,Klingensmith, Liane M.,Larrow, Jay F.,Lee, James K.,Martinelli, Michael J.,Miller, Larry M.,Moniz, George A.,Sakai, Kenichi,Tedrow, Jason S.,Hansen, Karl B.
, p. 133 - 141 (2010)
Two routes aimed at the manufacture of chiral exo-2-norbornyl thiourea (1) on large scale are described. The first approach involves five chemical steps and hinges on a classical resolution via diastereomeric salt formation. The synthesis utilizes amine 2 as the resolution handle. The second approach includes two chemical steps and a chiral chromatography of (±)-1. Despite the larger initial investment necessary to acquire the chiral stationary phase used in the chromatographic approach, the shorter reaction sequence and efficiency of the chromatographic separation make the second route a more attractive option for long-term applications.
