110901-92-3 Usage
Uses
Used in Medicinal Chemistry:
(1R,2S)-2-(3-Methoxy-phenyl)-cyclopropylamine is utilized as a key intermediate in the synthesis of pharmaceuticals, owing to its unique stereochemistry and structural features. It can be employed to develop new drugs with improved efficacy and selectivity.
Used in Drug Development:
(1R,2S)-2-(3-Methoxy-phenyl)-cyclopropylamine serves as a valuable building block in the design and development of novel therapeutic agents. Its potential biological activities and compatibility with various chemical moieties make it suitable for creating innovative drug candidates.
Used in Chemical Synthesis:
(1R,2S)-2-(3-Methoxy-phenyl)-cyclopropylamine can be used as a versatile reagent in organic synthesis, enabling the creation of a wide range of chemical products with diverse applications across different industries.
Further research is necessary to fully explore the properties and potential uses of (1R,2S)-2-(3-Methoxy-phenyl)-cyclopropylamine, as its current applications are based on its structural features and potential biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 110901-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,9,0 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 110901-92:
(8*1)+(7*1)+(6*0)+(5*9)+(4*0)+(3*1)+(2*9)+(1*2)=83
83 % 10 = 3
So 110901-92-3 is a valid CAS Registry Number.
110901-92-3Relevant academic research and scientific papers
N,N-dialkylated monophenolic trans-2-phenylcyclopropylamines: Novel central 5-hydroxytryptamine receptor agonists
Arvidsson,Johansson,Hacksell,Nilsson,Svensson,Hjorth,Magnusson,Carlsson,Lindberg,Andersson,Sanchez,Wikstrom,Sundell
, p. 92 - 99 (2007/10/02)
N,N-Dialkylated monophenolic derivatives of trans-2-phenylcyclopropylamine were synthesized and tested for central 5-hydroxytryptamine (5-HT) and dopamine (DA) receptor stimulating activity by use of a biochemical test method in rats. A hydroxy substituent in the 2- or 3-position of the phenyl ring was required for 5-HT-receptor stimulation. N,N-Diethyl or N,N-di-n-propyl substitution gave the most potent 5-HT-receptor agonists. The 4-hydroxy and 3,4-dihydroxy derivatives of trans-2-phenyl-N,N-di-n-propylcyclopropylamine were inactive at central DA and 5-HT receptors. In contrast, the corresponding 3-hydroxy derivative 18 and some of its derivatives weakly affected both DA and NE synthesis. Two of the most potent 5-HT-receptor agonists, trans-2-(2-hydroxyphenyl)-N,N-di-n-propylcyclopropylamine (8) and the 3-hydroxy isomer 18 were resolved into the enantiomers. The 1R,2S enantiomers of 8 and 18 displayed 5-HT activity, while the 1S,2R enantiomers were inactive. Compound (1R,2S)-18, but not (1R,2S)-8, weakly affected rat brain DA and NE synthesis.
