91247-06-2 Usage
Uses
Used in Pharmaceutical Research:
5,6-Dimethoxy-indan-1-ylamine is used as a research compound for its psychoactive properties, aiding in the development of new pharmaceuticals with potential therapeutic applications in mental health disorders.
Used in Psychopharmacology:
In the field of psychopharmacology, 5,6-dimethoxy-indan-1-ylamine is used as a study subject to understand its effects on the central nervous system, neurotransmitter activity, and behavior, contributing to the advancement of knowledge in psychoactive substances.
Used in Drug Development:
5,6-Dimethoxy-indan-1-ylamine is utilized in drug development as a potential candidate for psychoactive medications, with the aim of creating new treatments for various mental health conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 91247-06-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,4 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91247-06:
(7*9)+(6*1)+(5*2)+(4*4)+(3*7)+(2*0)+(1*6)=122
122 % 10 = 2
So 91247-06-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO2/c1-13-10-5-7-3-4-9(12)8(7)6-11(10)14-2/h5-6,9H,3-4,12H2,1-2H3
91247-06-2Relevant articles and documents
Method for synthesizing R type aminoindane
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Paragraph 0006; 0009, (2017/04/03)
The invention discloses a method for synthesizing R type aminoindane, namely R-5,6-dimethoxy-1-amino indan. The method specifically includes the steps that under the action of a catalyst, 5,6-dimethoxy-1-amino indanone is reduced and aminated to generate racemized 5,6-dimethoxy-1-amino indan, 5,6-dimethoxy-1-amino indan is combined with a racemization catalyst by means of lipase for dynamic kinetic resolution, and R-5,6-dimethoxy-1-amino indan is obtained. The method has the advantages of being easy to operate, wide in raw material source, good in product yield, high in resolution product optical purity and the like.
Indane dimerization products obtained by treatment of N-acylindan-1-amines with ethyl polyphosphate (EPP)
Moglioni, Albertina G.,Tombari, Dora G.,Moltrasio Iglesias, Graciela Y.
, p. 3459 - 3462 (2007/10/03)
This report describes the diverse dimeric products obtained by treatment of N-acylindan-1-amines with ethyl polyphosphate in chloroform-diethyl ether solution at 80°C for 8 h. Possible mechanisms for such reactions are discussed.
