218151-47-4 Usage
Uses
Used in Pharmaceutical Industry:
1H-Indene-1,2-diamine,2,3-dihydro-,(1S,2S)-(9CI) is used as a key intermediate in the production of certain antidepressant medications. Its unique structure and chemical properties contribute to the development of effective treatments for depression.
Used in Organic Compounds and Materials Development:
Due to its unique structure and chemical properties, 1H-Indene-1,2-diamine,2,3-dihydro-,(1S,2S)-(9CI) has potential applications in the development of new organic compounds and materials. It can be utilized to create innovative products with enhanced properties and functionalities in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 218151-47-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,8,1,5 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 218151-47:
(8*2)+(7*1)+(6*8)+(5*1)+(4*5)+(3*1)+(2*4)+(1*7)=114
114 % 10 = 4
So 218151-47-4 is a valid CAS Registry Number.
218151-47-4Relevant academic research and scientific papers
Asymmetric transfer hydrogenation of ketones using amino alcohol and monotosylated diamine derivatives of indane
Palmer, Matthew J.,Kenny, Jennifer A.,Walsgrove, Tim,Kawamoto, Aparecida M.,Wills, Martin
, p. 416 - 427 (2007/10/03)
A series of 1,2-amino alcohol and 1,2-monotosylated diamine derivatives of indane have been applied as ligands in the asymmetric ruthenium(II)-catalysed transfer hydrogenation reaction of a series of ketones. Of these, the cis-1-aminoindan-2-ol derivative gives some of the highest asymmetric inductions reported for any amino alcohol ligand in this application.
Synthesis of enantiomerically pure cis- and trans-1,2- diaminoindanes
Bit, Christelle,Mitrochkine, Anton A.,Gil, Gerard,Pierrot, Marcel,Reglier, Marius
, p. 3263 - 3273 (2007/10/03)
The four isomers of cis- and trans-1,2-diaminoindanes 5 and 11 were prepared in three steps and high enantiomeric excess by a key lipase- catalyzed selective transesterification of racemic cis-2-azido-1-indanol and trans-1-azido-2-indanol, respectively.
