91247-06-2 Usage
General Description
5,6-Dimethoxy-indan-1-ylamine is a chemical compound with the molecular formula C11H15NO2. It is a derivative of indanamine and is commonly used in research as a psychoactive drug. 5,6-DIMETHOXY-INDAN-1-YLAMINE has been studied for its potential use in the development of new pharmaceuticals with psychoactive properties, particularly in the treatment of mental health disorders. It is classified as a substituted phenethylamine and is structurally related to other psychoactive compounds such as mescaline and amphetamines. 5,6-Dimethoxy-indan-1-ylamine has been the subject of numerous studies to explore its effects on the central nervous system, including its potential role in modulating neurotransmitter activity and behavior. Overall, this chemical compound has garnered interest in the scientific community for its potential therapeutic applications and its role in advancing our understanding of psychoactive substances.
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
-
Paragraph 0008; 0011, (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.
