943516-55-0 Usage
Description
6,6-diMethyl-3-azabicyclo[3.1.0]hexane (Hydrochloride), also known as dimethylcyclopropanamine hydrochloride, is a bicyclic chemical compound derived from cyclopropane. It is characterized by its unique three-dimensional structure, making it a valuable building block in organic synthesis. 6,6-diMethyl-3-azabicyclo[3.1.0]hexane (Hydrochloride) is also recognized for its applications as a chiral auxiliary in asymmetric synthesis and as a ligand in metal-catalyzed reactions. Furthermore, it has been investigated for its potential pharmacological properties, such as its use as an antiviral and antibacterial agent.
Uses
Used in Pharmaceutical Synthesis:
6,6-diMethyl-3-azabicyclo[3.1.0]hexane (Hydrochloride) is utilized as a key intermediate in the synthesis of various pharmaceuticals due to its reactive and versatile bicyclic structure, which allows for the development of new drugs with improved therapeutic properties.
Used as a Chiral Auxiliary in Asymmetric Synthesis:
In the field of asymmetric synthesis, 6,6-diMethyl-3-azabicyclo[3.1.0]hexane (Hydrochloride) serves as an effective chiral auxiliary. It aids in enhancing the selectivity and yield of enantioselective reactions, contributing to the production of optically active compounds with desired chiral purity.
Used as a Ligand in Metal-Catalyzed Reactions:
6,6-diMethyl-3-azabicyclo[3.1.0]hexane (Hydrochloride) is employed as a ligand in metal-catalyzed reactions, where it plays a crucial role in stabilizing and directing the catalytic activity of metal complexes. This application is vital for the advancement of catalytic processes in organic synthesis.
Used in Antiviral and Antibacterial Applications:
6,6-diMethyl-3-azabicyclo[3.1.0]hexane (Hydrochloride) has been studied for its potential as an antiviral and antibacterial agent. Its unique structure and reactivity make it a promising candidate for the development of new therapeutic agents to combat viral and bacterial infections.
Check Digit Verification of cas no
The CAS Registry Mumber 943516-55-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,5,1 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 943516-55:
(8*9)+(7*4)+(6*3)+(5*5)+(4*1)+(3*6)+(2*5)+(1*5)=180
180 % 10 = 0
So 943516-55-0 is a valid CAS Registry Number.
943516-55-0Relevant articles and documents
HISTONE DEACETYLASE INHIBITORS AND COMPOSITIONS AND METHODS OF USE THEREOF
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Paragraph 0268, (2016/11/21)
Provided are certain histone deacetylase (HDAC) inhibitors of Formula (I), compositions thereof, and methods of their use.
AN IMPROVED PROCESS FOR THE PREPARATION OF RACEMIC 6, 6- DIMETHYL-3-AZABICYCLO-[3.1.0]-HEXANE AND ITS SALTS, A KEY RAW MATERIAL FOR HCV INHIBITOR.
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Page/Page column 38-39, (2012/05/04)
The present invention discloses an efficient and economical process for the preparation of racemic 6, 6-dimethyl-3-azabicyclo-[3.1.0]-hexane of formula I and its salts. The invention relates to the compounds of formulae I and II. The compound of formula I
