790208-54-7 Usage
General Description
1H-Inden-1-amine,6-fluoro-2,3-dihydro-,(1R)-(9CI) is a chemical compound with the molecular formula C9H10FN. It is an amine derivative, with a fluoro-substituted indene ring structure. 1H-Inden-1-amine,6-fluoro-2,3-dihydro-,(1R)-(9CI) is a chiral molecule, with the (1R) stereochemistry designation. It is a potential intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. The specific properties and applications of this compound may depend on its stereochemistry and further functionalization. Due to its potential biological and industrial relevance, it is of interest for further study and development in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 790208-54-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,0,2,0 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 790208-54:
(8*7)+(7*9)+(6*0)+(5*2)+(4*0)+(3*8)+(2*5)+(1*4)=167
167 % 10 = 7
So 790208-54-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H10FN/c10-7-3-1-6-2-4-9(11)8(6)5-7/h1,3,5,9H,2,4,11H2/t9-/m1/s1
790208-54-7Relevant articles and documents
Mapping the substrate scope of monoamine oxidase (MAO-N) as a synthetic tool for the enantioselective synthesis of chiral amines
Herter, Susanne,Medina, Florian,Wagschal, Simon,Benha?m, Cyril,Leipold, Friedemann,Turner, Nicholas J.
, p. 1338 - 1346 (2017/10/06)
A library of 132 racemic chiral amines (α-substituted methylbenzylamines, benzhydrylamines, 1,2,3,4-tetrahydronaphthylamines (THNs), indanylamines, allylic and homoallylic amines, propargyl amines) was screened against the most versatile monoamine oxidase (MAO-N) variants D5, D9 and D11. MAO-N D9 exhibited the highest activity for most substrates and was applied to the deracemisation of a comprehensive set of selected primary amines. In all cases, excellent enantioselectivity was achieved (e.e. >99%) with moderate to good yields (55–80%). Conditions for the deracemisation of primary amines using a MAO-N/borane system were further optimised using THN as a template addressing substrate load, nature of the enzyme preparation, buffer systems, borane sources, and organic co-solvents.
